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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539625Generated: October 31, 2026

Trimethyl phosphonoacetate → HCID 67043500, compound

https://huagongshe.com/reaction/539625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl phosphonoacetateHCID 80029—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 58200258HCID 58200258—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 67043500HCID 6704350081.6%

Reaction Steps

To a stirring room temperature suspension of LiCl (0.84 g, 19.8 mmol) in dry acetonitrile (50 mL) was added trimethyl phosphonoacetate (4 mL, 24.75 mmol). The resulting mixture was stirred for 5 minutes, then TEA (2.76 mL, 19.8 mmol) was added. The reaction mixture was stirred for 10 minutes, and then a solution of (4-oxo-1-phenyl-butyl)-carbamic acid benzyl ester (16.5 mmol) in acetonitrile (15 mL) was added. The reaction mixture was stirred at room temperature for 18 hours, then diluted with diethyl ether and saturated aqueous NH4Cl. The organic layer was separated, washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to an oil, which was chromatographed (5%-40% EtOAc in hexanes) to give 4.41 g (79%) of 4-benzyloxycarbonylamino-4-phenyl-butyric acid methyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871760B2
Source datasetuspto-grants-2014_10
ORD IDord-cbe3557726e34e04859247f4486392e3
Source noteuspto-grants-2014_10