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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859642Generated: November 1, 2026

Ammonium Chloride → Ethyl 4-benzyloxycarbonylamino-2,2-difluoro-3-hydroxy-5-phenylpentanoate

https://huagongshe.com/reaction/1859642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl bromodifluoroacetateHCID 69585—
ReactantBenzyl (1-oxo-3-phenylpropan-2-yl)carbamateHCID 11323549—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-benzyloxycarbonylamino-2,2-difluoro-3-hydroxy-5-phenylpentanoateHCID 1054937091.3%

Reaction Steps

To a mixture of the objective compound of step (10) (42.8 g, 0.151 mol), zinc dust (15.9 g, 0.243 mol) and THF (105 ml) was added ethyl bromodifluoroacetate (31.6 mL, 0.246 mol) with dropwise over 2 hours at 26˜49° C. The resulting mixture was stirred at room temperature for 2 hours. To this reaction mixture was added saturated ammonium chloride aqueous solution (110 mL), and the mixture was stirred for a few minutes. The obtained mixture was added to saturated ammonium chloride aqueous solution (650 mL) and extracted with ethyl acetate (500 mL, 2×300 mL). The extract was washed with saturated brine (400 mL), dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (2:1 hexane-ethyl acetate) to give 56.15 g of ethyl 4-benzyloxycarbonylamino-2,2-difluoro-3-hydroxy-5-phenylpentanoate as a light-yellow oil (a mixture of diastereomers, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528514B1
Source datasetuspto-grants-2003_03
ORD IDord-0bd87b20f67f4ce6a452470c93db8873
Source noteuspto-grants-2003_03