Reaktion #1949916

Reaktionsgleichung

1(5-methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehyde

Compound G

1(5-methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehyde

ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoate

Compound D

ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoate

n-BuLi

→

title compound

Ausbeute 90.0%

Ethyl 4-[1-(2,2-dimethoxyethyl)-2-{1-(5-methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-naphthalen-7-yl}-(E)-ethen-1-yl]-benzoate

Ausbeute 90.0%

Lösungsmittel

ether

THF

THF

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewas recooled to −78° C.
2. 2
   workup.STIRRINGThe mixture was stirred for 2 hours at −10° C.
3. 3
   Waschenwashed with brine (10 mL)
4. 4
   Trocknendried with MgSO4
5. 5
   Sonstigethe solvent was removed by distillation
6. 6
   Sonstigeto afford a cis and trans (E and Z) isomeric mixture
7. 7
   SonstigePurification by chromatography on silica gel of the crude material

Vorschrift

To a cold (−78° C.) solution of ethyl 4-(diethoxyphosphoryl-3,3-dimethoxypropyl)benzoate (Compound D, 1.4 g, 3.6 mmol), in THF (20 mL) was added n-BuLi (1.6 M solution in hexane, 2.5 mL, 4 mmol). The mixture was stirred for 20 minutes at −78° C. and 10 min. at −10° C. The reaction mixture was recooled to −78° C. and 1(5-methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-naphthaldehyde (Compound G, 650 mg, 2.3 mmol) in THF (4 mL) was added to it. The mixture was stirred for 2 hours at −10° C. and diluted with ether (100 mL), washed with brine (10 mL) dried with MgSO4 and the solvent was removed by distillation to afford a cis and trans (E and Z) isomeric mixture. Purification by chromatography on silica gel of the crude material afforded the title compound as an oil (˜90% purity).

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