Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443931Generated: October 31, 2026

Ethyl bromoacetate → HCID 23466036, compound

https://huagongshe.com/reaction/443931

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-2-one, 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 hydrochloric 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 numberUS04262013
Source datasetuspto-grants-1981_04
ORD IDord-1650dfa78e6841be9c428d243d70e6aa
Source noteuspto-grants-1981_04