Production Method 1

111-70-6

19037-72-0

141-93-5

931-88-4

575-37-1

2146-37-4

930-18-7

690-08-4

624-64-6

52161-57-6

16327-38-1

824-90-8

622-96-8

264-09-5

3404-65-7

616-12-6

691-38-3

824-22-6

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, , ,

Production Method 2

19037-72-0

141-93-5

930-18-7

17057-82-8

624-64-6

620-14-4

622-96-8

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, , ,

Cyclopentene,4,4-dimethyl- Raw materials

• 1-Heptanol

Cyclopentene,4,4-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)
• 1H-Indene,2,3-dihydro-1,2-dimethyl- (17057-82-8)
• 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)
• 3-Ethyltoluene (620-14-4)
• 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)

• 1. An extremely short synthesis of hirsutene
  Masahiko Iyoda,Takahiro Kushida,Sumiko Kitami,Masaji Oda J. Chem. Soc. Chem. Commun. 1986 1049
• 2. Index of subjects
  Annu. Rep. Prog. Chem. 1959 56 451
• 3. Synthesis and photoreaction of tricyclo[5.2.2.0?2,6]undecanes in the excited singlet (1 S??) state: a novel and stereospecific route to protoilludanoids
  Vishwakarma Singh,Uday Sharma S??) state: a novel and stereospecific route to protoilludanoids. Vishwakarma Singh Uday Sharma J. Chem. Soc. Perkin Trans. 1 1998 305
• 4. Domino retro Diels–Alder/Diels–Alder reaction: an efficient protocol for the synthesis of highly functionalized bicyclo[2.2.2]octenones and bicyclo[2.2.2]octadienones
  Santhosh Kumar Chittimalla,Hui-Yi Shiao,Chun-Chen Liao Org. Biomol. Chem. 2006 4 2267
• 5. A regioselective and stereospecific synthesis of allylsilanes from secondary allylic alcohol derivatives
  Ian Fleming,Dick Higgins,Nicholas J. Lawrence,Andrew P. Thomas J. Chem. Soc. Perkin Trans. 1 1992 3331

• 1759-81-5(Cyclopentene, 4-methyl-)
• 58049-91-5(Cyclopentene,3,3-dimethyl-)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)