Production Method 1

111-70-6

16327-38-1

141-93-5

931-88-4

575-37-1

2146-37-4

930-18-7

690-08-4

19037-72-0

624-64-6

52161-57-6

824-90-8

622-96-8

264-09-5

3404-65-7

616-12-6

691-38-3

824-22-6

14686-13-6

2808-79-9

Reaction Conditions

1.1 Catalysts: Vanadium ;  100 - 550 °C

Reference

Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

, World Intellectual Property Organization, , ,

Cyclobutene, 3,3-dimethyl- Raw materials

• 1-Heptanol

Cyclobutene, 3,3-dimethyl- Preparation Products

• 1,3-DIETHYLBENZENE (141-93-5)
• Cyclooctene (931-88-4)
• 1,7-Dimethylnaphthalene (575-37-1)
• Ethylidenecyclopentane (2146-37-4)
• Cyclopropane,1,2-dimethyl-, (1R,2S)-rel- (930-18-7)
• 2-Pentene,4,4-dimethyl-, (2E)- (690-08-4)
• Cyclopentene,4,4-dimethyl- (19037-72-0)
• 2-BUTENE (624-64-6)
• Benzene, 1-methyl-3-(1-methyl-2-propenyl)- (52161-57-6)
• Cyclobutene, 3,3-dimethyl- (16327-38-1)
• Benzene, 1-buten-1-yl- (824-90-8)
• 4-Ethyltoluene (622-96-8)
• 7H-Benzocycloheptene (264-09-5)
• 3-methyl-3-hexene (c,t) (3404-65-7)
• 2-Pentene, 3-methyl-,(2E)- (616-12-6)
• cis-4-Methyl-2-pentene (691-38-3)
• 4-Methylindan (824-22-6)
• 2-Heptene, (2E)- (14686-13-6)
• Cyclohexene,1,4-dimethyl- (2808-79-9)

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