181841. lajstromszámú szabadalom • Eljárás imidazolinon-származékok és belőle herbicid szerek előállítására

9

Táblázat folytatása

181841

10

Rí

r2

r3

X

Olvadáspont e

C-ban

CH3

CH(CH3)2-C(CH3)2C^CH

H

115 -116

ch3

CH(CH3)2

—CH(CH3)2

H

121 -122,5

ch3

CH(CH3)2-C(CH3)3

H

139,5-141

ch3

CH(CH3)2-ch2ch3

H

123 -124,5

ch3

CH(CH3)2-CH(CH3)C=CH

H

97 -104

ch3

CH(CH3)2-CH2C(C1)=CH2

H

114 -116

ch3

CH(CH3)2

-CH2CH2CsCH

H

127 -128

ch3

CH(CH3)2-CH(CH3)CH=CH2

H

94 - 98

(bomlik)

ch3-ch2ch2ch3-C(CH3)2CH=CH2

H

103,5-107

(bomlik)

ch3

ciklohexilcsoport-C(CH3)2CH=CH2

H

115 -120

(bomlik)

~(C H2)5--C(CH3)2CH=CH2

H

133,5-134,5

(bomlik)-CH(CH3 )CH2 ch2 ch2 ch 2 --ch2c=ch

H

168 -171

(bomlik)-ch3-CH(CH3)2-CH(CH3 )-C(CH3)=CH2

H

85 - 94

(bomlik)-ch3-CH(CH3)2-ch2ch=chch3

H

101 -112

(bomlik)-ch3

—CH(CH3)2-CH2C(CH3)SCH2

H

91 -102

(bomlik)-ch3-CH(CH3)2-CH2CH=C(CH3)2

H

107 -111-ch

3-CH(CH3)2

3-ciklohexenil-metilcsoport

H

100 -106

(bomlik)-ch3-CH(CH3)2-CH(CH=CH2)2

H

78 - 87

(bomlik)-ch3-CH(CH3)2-CH(CH3)-CH=CHCH3

H

89 -107

(bomlik)-CH(CH3)2 -CH(CH3)2-ch3

H

146 -147-(CH2),-ch3

H

164 -165

ch3

CH(CH3)2-CH2C(CH3)3

H

147 -148

ch3

ch(ch3)2

n—Ci ßH3 7—

H

79 - 81,5

ch3

CH(CH3)2-CH2CH2OCH3

H

87,5- 92,5

ch3

CH(CH3)2

furil-metil-csoport

H

122 -125

ch3

ch(ch3)2

n—CeH13—

H

84-86

ch3

CH(CH3)2

1,1 -dimetil-propil-csoport

H

87 - 89

ch3

CH(CH3)2

-CH2CH2OC2Hs

H

99 -100

ch3

CH(CH3)2-CH2CH=CH-C6Hs

H

120 -125

ch3

CH(CH3)2-CH2-CsC-C6H5

H

134,5-138

ch3

ch(ch3)2-ch2-c=c-ch3

H

125 -128

ch3

ch(ch3)2

1 -ciklopropil-etil-csoport

H

95 - 98

ch3

ch(ch3)2

—CH2—C=C—n—C7H15

H

94 - 96,5

ch3

ch(ch3)2-ch2cq3

H

143 -145

ch3

ch(ch3)2-C(C2H5)2CH=CH2

H

111,5-115,5

ch3

CH(CH3)2

3-metil-6-izopropil-l -ciklohexil-csoport

H

74 - 78

ch3

ch(ch3)2

etinil-ciklohexil-csoport

a

H

168 -169

ch3

CH(CH3)2-ch2-c=ch2

4(5)—CH3

128 -130

ch3

CH(CH3)2-ch3

4(5)—CH3

143 -151

ch3

CH(CH3)2-CH2-C=CH

4(5)—CH3

154 -159

ch3

ch(ch3)2

CH(CH3)2

H

153 -157,5

j-c-ch=ch2

1

CH(CH3)2

106 -108

ch3

CH(CH3)2

—C2H5 (+) izomer

H

ch3

CH(CH3)2 (—) izomer'-CH2-CsCH

H

134 -135

ch3

CH(CH3)2-ch2-c=ch2

H

120 -122

(+) izomer

1

Cl

ch3

CH(CH3)2

-CH(CH3)CH=CHCH3

4(5)—CH3

95-111

ch3

CH(CH3)2-ch3

3(6>-Cl

162-166

ch3

CH(CH3)2-CH2-CSCH

3(6)-Cl

164-166

ch3

ch(ch3)2-CH2-CSC-CH20H

H

132-134

5