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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277529Generated: October 30, 2026

Benzoate → Ethyl 4-[(7,8-dihydro-5,8,8-trimethylnaphth-3-yl)ethynyl]benzoate

https://huagongshe.com/reaction/277529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoateHCID 242—
Reactant4-[2-[5,6-Dihydro-5,5-dimethyl-8-[[(trifluoromethyl)sulfonyl]oxy]-2-naphthalenyl]ethynyl]benzoic acid ethyl esterHCID 12017638—
ReactantEthyl 4-[(7,8-dihydro-8,8-dimethyl-5-(1,1-dimethylethyl)naphth-3-yl)ethynyl]benzoateHCID 18314564—
ProductEthyl 4-[(7,8-dihydro-5,8,8-trimethylnaphth-3-yl)ethynyl]benzoateHCID 183145610.5%

Reaction Steps

Employing the same general procedure as for the preparation of ethyl 4-(7,8-dihydro-8,8-dimethyl-5-(1,1-dimethylethyl)naphth-3-yl)ethynyl]benzoate (Compound 71), 250 mg (0.52 mmol) of ethyl 4-[(5-trifluoromethylsulfonyloxy-7,8-dihydro-8,8-dimethylnaphth-3-yl)ethynyl]benzoate (Compound 66) was converted into the title compound (HPLC Partisil 10, 0.5% EtOAC-hexanes) using 70.2 mg (0.78 mmol) of cuprous cyanide, 33.2 mg (0.78 mmol) of lithium chloride and 34.5 mg (1.28 ml, 1.57 mmol) of methyllithium (1.22M solution in Et2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355806B1
Source datasetuspto-grants-2002_03
ORD IDord-6379556505b04ff39913b2110ef873eb
Source noteuspto-grants-2002_03