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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895706Generated: October 25, 2026

Ethyl bromopyruvate → HCID 22381051, compound

https://huagongshe.com/reaction/895706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantL-PenicillamineHCID 92863—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 22381051HCID 2238105134.5%

Reaction Steps

To a solution of L-penicillamine (298 mg, 2.0 mmol) in water (5 mL) and acetonitrile (5 mL) was added ethyl 3-bromopyruvate (0.25 mL, 390 mg, 2.0 mmol) slowly. To the resulted mixture was added sodium bicarbonate aqueous solution till the pH about 5. Acetonitrile was removed under vacuum and some more water was added. The solution was extracted with methylene chloride. The water phase was separated and freeze-dried under high vacuum. The residue was chromatographed (silica gel, methylene chloride-methanol-acetic acid 100:5:0.3 to 100:10:0.3) to give 150 mg of product (yield 31%). 1HNMR (300 Hz, D3COD) δ (ppm) 6.17 (s, 1H), 4.23 (q, J=7.1 Hz, 2H), 3.79 (s, 1H), 1.48 (s, 3H), 1.31 (t, J=7.1 Hz, 3H), 1.29 (s, 3H). 13CNMR (75 Hz, D3COD) δ (ppm) 173.8, 164.0, 128.0, 102.4, 64.1, 62.2, 41.2, 28.3, 25.2, 14.7 ppm. MS (ESI) m/z 268 (M+Na, 100), 246 (M+1, 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916850B2
Source datasetuspto-grants-2005_07
ORD IDord-cb77d3d769ad426b93264f6323dd9ee8
Source noteuspto-grants-2005_07