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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415909Generated: October 31, 2026

Ethyl Acetate → methyl (Z)-3-{3-[5-(tert-butyldimethylsilyloxy)-pentyloxy]-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl}-2-butenoate

https://huagongshe.com/reaction/1415909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10900307HCID 10900307—
ReactantHCID 86754091HCID 86754091—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Productmethyl (Z)-3-{3-[5-(tert-butyldimethylsilyloxy)-pentyloxy]-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl}-2-butenoateHCID 86754090—

Reaction Steps

A mixture of tetrakis(triphenyl-phosphine)palladium (155 mg), 3-[5-(tert-butyldimethylsilyloxy)pentyloxy]-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthaleneboronic acid (300 mg, 0.67 mmol), a 2M solution of potassium carbonate in water (0.67 ml) and methyl (Z)-3-iodo-2-butenoate (Ma, S. & Lu, X.; J. Chem. Soc. Chem. Com., pp. 1643-1644 (1990)) (182 mg) in dimethoxyethane (DME) (10 ml) was heated to reflux for 24 h. The solution was poured into a mixture of water and ethyl acetate. The organic phase was washed twice with water, dried over magnesium sulfate and concentrated in a rotary evaporator under vacuum at 40° C. The desired compound was purified by flash chromatography on a silica column.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910508
Source datasetuspto-grants-1999_06
ORD IDord-bb5b252a16af4043b7f0f2fda92da538
Source noteuspto-grants-1999_06