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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607620Generated: October 27, 2026

Phenethyl bromide → Tert-butyl 3-oxo-2-phenethylbutanoate

https://huagongshe.com/reaction/1607620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantTert-butyl acetoacetateHCID 15538—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductTert-butyl 3-oxo-2-phenethylbutanoateHCID 13195717—

Reaction Steps

Sodium (2.3 g; 0.10 mol) was allowed to react with dry ethanol (50 ml) under nitrogen. The resulting clear solution was cooled (ice bath) and t-butyl acetoacetate (15.8 g; 0.10 mol) was added during 10 minutes with stirring. After 10 minutes, 2-(bromoethyl)benzene (18.5 g; 0.10 mol) was added during 30 minutes. The resulting solution was heated at reflux for 4 hours, then cooled and filtered. After concentration, the residue was partitioned between water and ether, and the ether layer was dried (MgSO4) and concentrated. Distillation of the residue gave 21.0 g (0.080 mol; 80%) of the title product; bp 110°-120° (0.3 mm). NMR (CDCL3); 1.45 (9H,s), 2.17 (3H,s), 1.8-2.4 (2H,m), 2.5-2.7 (2H,m); 3.28 (1H,J=7); 7.2-7.4 (5H, broad s). MS (m/e); 262 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866087
Source datasetuspto-grants-1989_09
ORD IDord-84bf18827424485dbe91373cdf3c6b91
Source noteuspto-grants-1989_09