HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326922Generated: October 27, 2026
Triphenylphosphine → Methyl 3(S)-(acetylthio)butanoate
https://huagongshe.com/reaction/326922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Methyl 3-hydroxybutyrate, (R)- | HCID 2724279 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3(S)-(acetylthio)butanoate | HCID 15289607 | — |
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 25° 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05270324 |
|---|
| Source dataset | uspto-grants-1993_12 |
|---|
| ORD ID | ord-b31bf3fe89364d939c22c5f9abf6f03b |
|---|
| Source note | uspto-grants-1993_12 |
|---|