HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638184Generated: November 4, 2026
Hexane → (4S)-4-propan-2-yl-3-prop-2-enoyl-1,3-oxazolidin-2-one
https://huagongshe.com/reaction/1638184
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (4S)-4-(propan-2-yl)-1,3-oxazolidin-2-one | HCID 7157133 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4S)-4-propan-2-yl-3-prop-2-enoyl-1,3-oxazolidin-2-one | HCID 10954182 | 89% |
Reaction Steps
Production in a way similar to: D. A. Evans, K. T. Chapman, J. Bisha J. Am. Chem. Soc. 1988, 110, 1238; A Studer, T. Hintermann, D. Seebach Helv. Chim. Acta 1995, 78, 1185. 6.88 ml of a 1.6M solution of n-BuLi in hexane (11.0 mmol) is slowly added to a solution of 1.299 g (10.0 mmol) of (S)-4-isopropyl-oxazolidin-2-one in 15 ml of absolute THF at -78° C. The solution is stirred for 30 minutes at -78° C.; 1.22 ml (15.0 mmol) of acrylic acid chloride is added drop by drop; it is allowed to reach room temperature and hydrolyzed with 50 ml of saturated NH4Cl solution. It is extracted three times with 50 ml of Et2O each. After drying on MgSO4, the solvent is removed. By flash-chromatographic purification with pentane/Et2O (10:1), 1.63 g (8.9 mmol, 89%) of 20 is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06043372 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-56cc7c4492014dbdabe389f3f4ebc78a |
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| Source note | uspto-grants-2000_03 |
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