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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433080Generated: November 2, 2026

Water → 5-Benzyloxycarbonylamino-4-bromo-3-oxo-pentanoic acid ethyl ester

https://huagongshe.com/reaction/1433080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 5-benzyloxycarbonylamino-3-oxo-pentanoateHCID 15195445—
SolventAcetic AcidHCID 176—
Product5-Benzyloxycarbonylamino-4-bromo-3-oxo-pentanoic acid ethyl esterHCID 86592562—

Reaction Steps

5-Benzyloxycarbonylamino-3-oxo-pentanoic acid ethyl ester (1.0 g, 3.4 mmol) is dissolved in glacial acetic acid (10 mL) and pyridinium bromide perbromide (1.1 g, 3.4 mmol) of is added. The reaction stirred 16 hrs and then poured into H2O (100 mL) and extracted with ethyl acetate (2×100 mL). The organic layers are combined and washed with H2O (2×100 mL) and with brine (2×100 mL). The organic layer is dried over MgSO4, filtered and reduced to an oil by rotary evaporation. The crude product is purified by flash chrom-atography on silica gel using 25% ethyl acetate/hexane as the eluent to provide 5-benzyloxycarbonylamino-4-bromo-3-oxo-pentanoic acid ethyl ester. 1H NMR (300 MHz, CDCl3) δ 7.34 (s, 5H), 5.27 (m, 1H), 5.09 (s, 2H), 4.67 (t, 1H), 4.17 (q, 2H), 3.72 (m, 4H), 1.27 (t, 3H); MS (ion spray) 372 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-2e84e979a33048efa6560b484bfcfaa9
Source noteuspto-grants-2009_11