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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132613생성일: 2026년 10월 24일

Pentanoic Acid → (4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-one

https://huagongshe.com/ko/reaction/132613

반응식

참여 물질

역할이름HCID투입량
반응물Pentanoic AcidHCID 7991—
반응물TriethylamineHCID 8471—
반응물Pivaloyl chlorideHCID 62493—
반응물Lithium ChlorideHCID 433294—
반응물4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-HCID 853161—
용매TetrahydrofuranHCID 8028—
생성물(4S,5R)-4-Methyl-3-pentanoyl-5-phenyl-oxazolidin-2-oneHCID 69269495—

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388023B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-17bf84a0f9ce45c9bc7ffc3dad778df2
출처 메모uspto-grants-2008_06