188271. lajstromszámú szabadalom • Anilin-származékokat tartalmazó gyomirtószerek és eljárás anilin-származékok előállítására

188; 271

Sorszám

R1

Y

R2

R3

X

A

Zn

Olvadáspont,

■C/nD

294.

N(OCHj) (CH,)

H

H

H

O

— CH,—CH(CH,)—O—

2,4—Cl,

295.

N(OCHs) (CH,)

H

H

H

O

—CH, — CH,—O—

2.4,6 —Cl,

44 46

296.

N(OCH3) (CH,)

H

H

H

O

—CH, —CH,—O—

3 —CF,

297.

N(OCHj) (CH,)

H

H

CH,

O

—CH, —CH,—0 —

3—CF,

298.

N(OCH3) (CH,)

H

H

H

O

—CH,—CH,—O —

2—CH,. 4—Cl

299.

N(OCH3) (CH3)

H

H

CH,

O

— CH, —CH,—O—

2—CH,. 4 —Cl

300.

N(OCH,) (CH,)

H

H

H

O

— CH, —CH, —O —

3 — OCH,

301.

N(OCH,) (CH,)

H

H

CH,

O

— CH,—CH,—O —

3-OCH,

302.

N(OCH,) (CH,)

H

H

H

O

— CH, —CHZ—

H

—O—CH,-CH,

303.

N(OCH,) (CH,)

H

CH,

H

O

—CH,—CH,—

H

— O —CH, —CH,

304.

N(OCH,) (CH,)

H

H

H

O

— CH,—CH,—CH,—O—

H

305.

N(OCH,) (CHS)

H

CH,

H

O

— CH, — CH,— CH,—O —

H

306.

N(OCH,) (CH,)

H

H

H

0-(CH,).—O—

H

307.

N(OCH,) (CH3)

H

CH,

H

0

—(CH,).-0-H

308.

N(OCH,) (CH,)

H

H

H

0

—CH,—CH,—O—CH,—

2,4—Cl,

309.

N(OCH,) (CH,)

H

CH,

H

0

— CH,—CH,—O—CH,—

2,4—0,

310.

N(OCH,) (CH,)

H

H

H

0

— CH,—CH,—O—CH,—

H

311.

N(OCH,) (CH,)

H

CH,

H

0

— CH,—CH,—O —CH,—

H

312.

N(OCH,) (CH,)

H

H

H

o

— (CH,), O CH,

H

313.

NfOCH,) (CH,)

H

CH,

H

0

— (CH,),—O—CH,

H

314.

N(OCH,) (CH,)

4 —Cl

H

H

o

—CH,~CH,—O—

H

315,

N(OCH,) (CH,)

4—Cl

CH,

H

0

—CH, —CH,—O—

H

316.

N(OCH,) (CH,)

4—Cí

H

H

o

—CH,—CH(CH,)—O—

H

317.

NlOCH,) (CH,)

4—Cl

CH,

H

0

—CH,—CH(CH,)—O —

H

318.

N(OCH,) (CH,)

4—Cl

H

H

0

— CH,— CH,—O—

2,4—Cl,

319.

N(OCH,) (CH,)

4—Cl

CH,

H

0

— CH,—CH,—O —

2.4—0,

320.

N(OCH,) (CH,)

4—Cl

CH,

CH,

0

— CH,—CH,—O —

2.4—Cl,

321.

N(OCHj) (CH,)

4—Cl

H

H

0

— CH,—CH(CHj)—O—

2.4—0,

322.

N(OCH,) (CH,)

4—Cl

CH,

H

0

— CH,— CH(CHj)—O—

2,4 —Cl,

323.

N(OCH,) (CH,)

4—Cl

CH,

CH,

o

—CH,—CH(CH,)—O —

2.4 — 0,

324.

N(CH,)j

H

H

H

0

— CH,—CH,—

H

325,

N(CH,),

H

H

H

0

—CH,—CH,—O—

H

326.

N(CH,),

H

CH,

H

o

—CH,—CH,—O—

H

327.

N(CH,),

H

H

H

0

— CH,—CH,—O—

4 —Cl

328.

N(CH,)i

H

CH,

H

o

— CH,—CH,—O—

4—0

329.

N(CH,),

H

H

H

0

— CH,—CH, —O —

2.4—0,

330.

N(CH,),

H

CH,

H

0

— CH,—CH, —0 —

2.4—0,

331.

N(CH,),

H

H

H

o

—CH,—CH(CH,)—0—

H

332.

N(CH,),

H

CH,

H

0

— CH,—CH(CH,)—0—

H

333.

N(Cfíj),

4—Cl

H

H

0

— CH,—CH(CH,)—0 —

H

334.

N(CHj),

4 —Cl

CH,

H

0

—CH,—CH(CH,)—0—

H

335.

N(CH,),

H

H

H

o

— CH(CH,)—CH,—O—

H

336.

N(CH,)a

4 —Cl

H

H

0

— CH(CH,)—CH,—O—

H

337.

N(CH,) (CH,)

H

H

H

0-CH,-3.4—0,

338.

N(CH,),

H

H

H

0-CH,-3.4 — 0,

339.

N(CH,)j

H

CH,

H

o-CH,-3.4—0,

340.

N(OCH,) (CH,)

H

CH,

H

o

~CH,

3.4—0,

341.

N(OCH,) (CH,)

4—Cl

H

H

0-CH,-3.4 —Cl,

87 89

342.

NlOCH,) (CH,)

4—Cl

CH,

H

o

— CH,—

3.4—0,

343.

N(CH,),

4—C!

H

H

o

— CH,—

3.4—0,

87 92

344,

N(CH,),

H

H

H

o-CH,-4 — CH,

345.

N(CH,)j

4 —Cl

CH,

H

o

— CH,—

H

346.

etil

H

H

H

0

— CH,—CH, —O—

H

347.

etil

H

CH,

H

o

—CH, —CH,—O—

H

348.

etil

H

H

H

0

—CH, — CH2—O—

2.4—0,

349.

etil

H

CH,

H

o

—CH, —CH,—O—

2,4—0,

350.

etil

4—Cl

H

H

o

—CH, —CH,—O —

H

351.

etil

4—Cl

CH,

H

o

—CH, —CH,—O —

H

352.

etil

4—Cl

H

H

o

—CH, —CH,—O —

2.4—0,

353.

4—Cl

CH,

H

o

—CH, —CH, —O —

2.4—0,

354.

N(OCH,) (CH3)

4—Cl

H

H

o

— CH,—CH,—O—CH,

H

355.

N(OCH,) (CH,)

4 —Cl

CH,

H

0

— CH, —CH,—0 —CH,

H

356.

NlOCH,) (CH,)

4 —Cl

H

H

0

(CH,), 0 CH,

H

357.

N(OCH,) (CH,)

4—Cl

CH,

H

0

—(CH,),—0 CH,

H

358.

N(CH,),

H

H

H

0

(CH,), 0 CH,

H

359.

N(CH,),

H

H

H

o

—CH,—CH,—O—CH,

H

360.

N(CH,),

H

H

H

0-CH,H

113 116

36 f.

N(C'H,)i

H

H

H

0

— CH,—

H

73 75

362.

N(CH.,)j

H

CH,

H

o-CH,-4—CH,

73 74

363.

N(CH,),

H

CH,

H

o-CH,-4—0

olaj

364.

NIC)),),

H

H

H

o-CH,-4-(2-CI-4-CF3-fenoxi)

365.

N(CHj),

H

H

H

o-CH,-3-(2*C1-4-CF,-fenoxi)

366.

N(CH,)j

H

H

H

0-CH,-4-( 2.4-0,-fenoxi)

367.

N(CH,),

H

H

H

0

— CH,—

3-( 2,4-0,-fenoxi)

368.

— C(CH,)— CH,

H

CH,

H

o

—CH,—

H

47 48

369.

N(OCHj) (CH,)

H

H

H

o

— CH,—

4-<2-Cl-4-CF,-fenoxi)

58 62

370.

N(OCHj) (CH,)

H

CH,

H

0

—CH,—

4-(2-0-4-CF,-fenoxi)

371.

NlOCH,) (Cll,)

4 —Cl

H

H

0-CH,-4-(2-Cl-4-CF,-fenoxi)

372.

N(OCH,) (CH,)

H

H

H

o

—CH,—

3-(2-Cl-4-CF,-fenoxi)

= 1.5616

373.

N(OCH,) (CH,)

H

CH,

H

o

— CH,—

3-(2-Cl-4-CF,-fenoxi)

374.

N(OCH,( (CH,)

4—Cl

H

H

o

— CH,—

3-(2-Ci-4-CF3-fenoxi)

375.

N(OC,H,) (C,H,)

H

H

H

o-CH,H

= 1.5620

376.

NH-ciklopropil

H

CH,

H

0

— CH,—

4—0

szívós olaj

377.

etil

H

H

H

0

. —CH,—CH,—0 —CH,

H

378.

etil

H

H

H

o

— CH, —CH,—0—CH,- H

379.

N(OCH,) CH,

H

H

H

0

— CH(CH,)—

4-fenil

380.

N(CH,),

H

H

H

o

—CH(CH,)—

4-fenil

8