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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444058Generated: November 1, 2026

Ethyl 5-bromovalerate → HCID 22815604, compound

https://huagongshe.com/reaction/444058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-bromovalerateHCID 84580—
ReactantEthyl cysteinate hydrochlorideHCID 2723617—
ReactantSodiumHCID 5360545—
ReactantMonosodium phosphateHCID 23672064—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductHCID 22815604HCID 22815604—

Reaction Steps

L-Cysteine ethyl ester hydrochloride (18.6 g; 0.10 mole) was added to a solution of sodium (4.6 g; 0.20 g.a) in ethanol (320 ml, absolute), stirred 15 minutes and then the solvent removed in vacuo. To a solution of the residual sodium salts in dry dimethylsulphoxide (200 ml) was added ethyl 5-bromovalerate (21.0 g; 0.10 mole) in a single portion with stirring. The reaction mixture was allowed to stand at room temperature overnight, warmed on a steam bath for 5 mins. and then poured onto water (300 ml) containing sodium dihydrogen phosphate (1 g). The oil was extracted with ether (3×), the combined extracts washed with water and dried over MgSO4. The solvent was removed in vacuo yielding the product as a pale yellow oil which was used in Example 70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04262128
Source datasetuspto-grants-1981_04
ORD IDord-f4c9c5c8433547e8964623eafb90fb57
Source noteuspto-grants-1981_04