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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22447생성일: 2026년 10월 24일

Water → 2-Mercapto-4-Methylpentanoic Acid

https://huagongshe.com/ko/reaction/22447

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sulfuric AcidHCID 1118—
반응물Potassium BromideHCID 253877—
반응물D-LeucineHCID 439524—
생성물2-Mercapto-4-Methylpentanoic AcidHCID 13633258—

반응 단계

A solution of D-Leucine (5 g) and potassium bromide (114 g) in 400 ml of 2.5 N H2SO4 was cooled to -5° C. in an ice salt bath. A cold solution of NANO2 (30 g/70 ml water, 0°-50° C.) was added dropwise with stirring. The reaction was allowed to proceed for ~14 hours at room temperature. The reaction was then extracted with 75 ml portions of ether three times. The ether extract was dried over anhydrous sodium sulfate. The solution was filtered and the ether was evaporated. The resulting clear oil, 2-bromo-4-methylpentanoic acid (Martin and Greco, (1968) J. Org. Chem. 33, 1275-1276) (18 g) was committed to a 250 ml solution of 33% sodium trithiocarbonate with stirring at 0° C. The reaction was stirred for 48 hrs and then acidified at 0° C. with judicious addition of 10N H2SO4. The acidified solution was then extracted with 75 ml portions of ether three times. The ether extracts were dried over anhydrous sodium sulfate, and subsequently the ether was removed in vacuo. The resulting yellowish oil (17 g) was vacuum distilled. The final yield was 15.3 g of (S)-2-mercapto-4-methylpentanoic acid; b.p. 92-93 (0.75 mmHg); [α]D 25=-23.2 (cl,MeOH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428019
출처 데이터셋uspto-grants-1995_06
ORD IDord-ec9f388bfd9b4df79ccb6906c2ab361f
출처 메모uspto-grants-1995_06