HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382213Generated: October 28, 2026
2-Thiopheneacetyl chloride → HCID 18341340, compound
https://huagongshe.com/reaction/382213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiopheneacetyl chloride | HCID 162362 | — |
| Reactant | (S)-4-Benzyl-2-oxazolidinone | HCID 736225 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18341340 | HCID 18341340 | 53% |
Reaction Steps
To a solution of (S)-(-)-4-benzyl-2-oxazolidinone (350 mg, 2.00 mmol) in dry THF (10 mL) at −30° C. was added dropwise n-butyllithium (2.59 M in hexanes, 0.8 mL). The mixture was cooled to −78° C. and treated with 2-thiopheneacetyl chloride (0.25 mL, 2 mmol). After stirring at −78° C. for 45 minutes, the mixture was allowed to warm to ambient temperature and stir for 1 hour. The mixture was diluted with hexanes (10 mL), quenched with 1M pH7 phosphate buffer, and stirred for 45 minutes. The layers of the resultant biphasic mixture were separated and the aqueousueous phase extracted with EtOAc. The combined organic layers were washed with 0.5N aqueous HCl two times, saturated aqueous NaHCO3 two times, and brine, dried over Na2SO4, and concentrated to provide a crude residue which was purified via flash column chromatography with 20% EtOAc/hex as eluant to yield 319 mg (53%) of 4(S)-benzyl-3-(2-thien-2-yl-acetyl)-2-oxazolidinone as a tan solid, mp 56-9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06306892B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-9c1dafa47a624059b372e5cc3d2ee4b2 |
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| Source note | uspto-grants-2001_10 |
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