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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342002Generated: October 26, 2026

Triphenylphosphine → Methyl 3(S)-(acetylthio)butanoate

https://huagongshe.com/reaction/342002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Thiopheneacetic acidHCID 15970—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantMethyl 3-hydroxybutyrate, (R)-HCID 2724279—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3(S)-(acetylthio)butanoateHCID 15289607—

Reaction Conditions

Temperature-23 °C

Reaction Steps

To a -23° C. solution of PPh3 (40 mmol, 10.48 g) in THF (100 mL) was added diethyl azodicarboxylate (40 mmol, 6.28 mL) dropwise and the mixture was stirred at -23° C. for 16 hours, during which time a white precipitate was obtained. A THF (30 mL) solution of methyl 3(R)-hydroxybutanoate (20 mm, 2.36 g) and thiolacetic acid (20 mmol, 2.85 mL) was slowly added and the mixture was allowed to slowly warm to 25° C. and was stirred 16 h at 250° C. Most THF was removed in vacuo and EtOAc (10 mL) and hexanes (100 mL) were added. Insolubles were removed by filtration and the residue was purified by chromatography on silica gel to afford the title compound. [α]D25 =-21° (c=3, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856322
Source datasetuspto-grants-1999_01
ORD IDord-0ac75f8f9fca47a4bd67279d1e38a2df
Source noteuspto-grants-1999_01