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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481230Generated: October 25, 2026

Ethyl bromoacetate → (+/-) Ethyl 2-(1-hydroxy-1,2,3,4-tetrahydro-4,4-dimethyl-7-bromo-naphthalen-1-yl)acetate

https://huagongshe.com/reaction/481230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10753357—
CatalystZincHCID 23994—
SolventBenzeneHCID 241—
Product(+/-) Ethyl 2-(1-hydroxy-1,2,3,4-tetrahydro-4,4-dimethyl-7-bromo-naphthalen-1-yl)acetateHCID 22571522—

Reaction Steps

To a suspension of Zn (1.20 g, 18.4 mmol) in 10 mL benzene at 100° C. was slowly added a solution of ethyl 2-bromoacetate (658.0 mg, 3.94 mmol) and 3,4-dihydro-4,4-dimethyl-7-bromo-naphthalen-1(2H)-one (Compound G, 500.0 mg, 1.97 mmol) in 20.0 mL benzene. The resulting mixture was heated for 2 h, cooled to room temperature, and the solution decanted from the residual solids. The solids were washed with EtOAc and the combined organic layers were washed with cold 15% H2SO4, saturated aqueous NaHCO3, and saturated aqueous NaCl before being dried over MgSO4. Removal of the solvents undr reduced pressure and column chromatography (10% EtOAc-hexanes) afforded the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653483B1
Source datasetuspto-grants-2003_11
ORD IDord-ad7e35d0fa604e16a2706e6017c28c1f
Source noteuspto-grants-2003_11