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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650832Generated: October 30, 2026

Sodium Chloride → HCID 15056132, compound

https://huagongshe.com/reaction/1650832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantEthyl bromoacetateHCID 7748—
ReactantTriethylamineHCID 8471—
ReactantHCID 57114383HCID 57114383—
SolventDimethylformamideHCID 6228—
ProductHCID 15056132HCID 15056132—

Reaction Steps

To a solution of (2S,4R)-2-aminomethyl-4-t-butyldimethylsilyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (5 g) and triethylamine (1.87 ml) in N,N-dimethylformamide (50 ml) was dropwise added ethyl bromoacetate (1.49 ml) at ambient temperature with stirring. The mixture was stirred at 40° C. for 30 minutes and then allowed to stand at ambient temperature for 6 hours. The reaction mixture was poured into saturated aqueous sodium chloride (100 ml) and extracted twice with ethyl acetate (100 ml). The extract was washed with saturated aqueous sodium chloride, dried over magnesium sulfate and evaporated in vacuo. The resulting residue was subjected to a column chromatography on silica gel (100 g) eluting with a mixture of dichloromethane and acetone (20:1 V/V). The fractions containing the desired compound were collected and evaporated in vacuo to give (2S,4R)-4-t-butyldimethylsilyloxy-2-[(ethoxycarbonylmethyl)aminomethyl]-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (3.52 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925838
Source datasetuspto-grants-1990_05
ORD IDord-cfcc70ac199f456a8540edc2b6eb14d3
Source noteuspto-grants-1990_05