참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pentanoic Acid | HCID 7991 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Pivaloyl chloride | HCID 62493 | — |
| 반응물 | Lithium Chloride | HCID 433294 | — |
| 반응물 | 4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)- | HCID 853161 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-one | HCID 69269495 | — |
반응 단계
To a 0° C. stirred solution of valeric acid (3.83 mL, 35.2 mmol) and Et3N (14.7 mL, 106 mmol) in dry THF (175 mL) was added trimethylacetyl chloride (5.29 mL, 42.3 mmol) dropwise. The mixture was stirred at 0° C. for 1 hour and (4S,5R)-(−)-4-methyl-5-phenyl-2-oxazolidinone (7.50 g, 42.3 mmol) was added followed by LiCl (1.79 g, 42.3 mmol). The reaction was warmed to room temperature overnight with good stirring. The mixture was filtered and the filtrate was concentrated under reduced pressure. Et2O (75 mL) was added to the residue, which was washed with sat. NaHCO3 (3×40 mL), 1N HCl (3×40 mL), and brine (2×40 mL). The organic phase was dried over MgSO4, filtered and concentrated under reduced pressure to give a quantitative yield of crude product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07388023B2 |
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| 출처 데이터셋 | uspto-grants-2008_06 |
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| ORD ID | ord-17bf84a0f9ce45c9bc7ffc3dad778df2 |
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| 출처 메모 | uspto-grants-2008_06 |
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