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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323536Generated: October 25, 2026

Penicillin G → (S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate

https://huagongshe.com/reaction/323536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPenicillin GHCID 5904—
ReactantSodium HydroxideHCID 14798—
ReactantRacemic ethyl 3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoateHCID 20644236—
SolventPhosphateHCID 1061—
Product(S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoateHCID 54332815—

Reaction Steps

Racemic ethyl 3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate (1g) was suspended in phosphate buffer (250 mL, 0.01 molar, prepared from 0.1 molar pH 7.24 solution obtained from sigma). The pH of the solution was adjusted 7.8 using dilute sodium hydroxide. Under slow stirring, 100 units of immobilized penicillin G acylase (Boehringer-Mannheim) was added. The reaction mixture was stirred at room temperature for 48 hours. The reaction mixture was extracted with ethyl acetate (75 mL×3). The organic extracts were combined, dried over sodium sulfate, filtered and evaporated to dryness to give the desired amide, (S)-ethyl-3-(phenoxyacetamido)-5-(trimethylsilyl)-4-pentynoate. The immobilized enzyme was filtered off from the aqueous phase using Whatman No.1 filter paper. The pH of the aqueous phase was adjusted to 8.0 using dilute sodium hydroxide, and extracted with ethyl acetate (75 mL×3). The extracts were combined, dried over sodium sulfate, filtered and evaporated to dryness to give the desired amine, (R)-ethyl-3-amino-5-(trimethylsilyl)-4-pentynoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214609B1
Source datasetuspto-grants-2001_04
ORD IDord-a134e06962504c938f001d697517685b
Source noteuspto-grants-2001_04