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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049695Generated: November 3, 2026

Ethyl bromoacetate → HCID 23466036, compound

https://huagongshe.com/reaction/2049695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant5-Oxo-1-phenylhexan-3-yl acetateHCID 23466017—
CatalystZincHCID 23994—
ProductHCID 23466036HCID 23466036—

Reaction Steps

Using 1.48 g of 4-acetoxy-6-phenylhexan-2one, 1 ml of ethyl bromoacetate and 0.62 g of zinc, the reaction and the purification of the product were carried out according to the method described in Example 1 (a) affording 1.03 g of ethyl 3-hydroxy-3-methyl-5-acetoxy-7-phenylheptanoate. The ester (0.90 g) thus obtained was dissolved in 5 ml of methanol and 2 ml of 4 N sodium hydroxide was added thereto. The mixture was stirred for 4 hours at room temperature, acidified by the addition of 4 N hydrocholoric acid, 5 ml of ethyl acetate was added and the mixture was stirred for 3 days. The usual treatment of the organic solvent layer afforded 400 mg of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198425
Source datasetuspto-grants-1980_04
ORD IDord-e879f96c50ab4a0cbdd44eafbddbe4ad
Source noteuspto-grants-1980_04