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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300660Generated: October 31, 2026

Sodium Formate → Methyl 4-(chlorobenzoyl)-4-hydroxybutyrate

https://huagongshe.com/reaction/2300660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FormateHCID 2723810—
ReactantMethyl 4-bromo-4-(chlorobenzoyl)butyrateHCID 18376473—
SolventMethanolHCID 887—
ProductMethyl 4-(chlorobenzoyl)-4-hydroxybutyrateHCID 18376491100.2%

Reaction Steps

A mixture of methyl 4-bromo-4-(chlorobenzoyl)butyrate (89.5 g), sodium formate (76.2 g) and methanol (400 ml) was stirred under reflux for 12 hours. The reaction mixture was concentrated, and water was added to the resulting residue and then extracted with ethyl acetate. The ethyl acetate layer was washed with water, and dried (MgSO4). The solvent was evaporated to give methyl 4-(chlorobenzoyl)-4-hydroxybutyrate (72.0 g, 100%) as an oily substance. This oily substance (72.0 g) was dissolved in tetrahydrofuran (400 ml), pyridine (22.2 g) was added thereto, and thereafter phenyl chlorocarbonate (43.8 g) was dropwise added thereto with cooling with ice. After the reaction mixture was stirred at room temperature for 1 hour, water was added to the reaction mixture and then extracted with ethyl acetate. The ethyl acetate layer was washed with 2 N hydrochloric acid and then with water, and dried (MgSO4). The solvent was evaporated, and the crystals thus precipitated were collected by filtration to obtain methyl 4-(4-chlorobenzoyl)-4-phenoxycarbonyloxybutyrate (61.2 g, 58%). This was recrystallized from methanol to give colorless prisms. mp 97-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498179B1
Source datasetuspto-grants-2002_12
ORD IDord-e227f23b67564292b29513c3b4bc2a62
Source noteuspto-grants-2002_12