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HRID 22447作成日:2026年10月26日

Water → 2-Mercapto-4-Methylpentanoic Acid

https://huagongshe.com/reaction/22447

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sulfuric AcidHCID 1118—
反応物Potassium BromideHCID 253877—
反応物D-LeucineHCID 439524—
生成物2-Mercapto-4-Methylpentanoic AcidHCID 13633258—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428019
出典データセットuspto-grants-1995_06
ORD IDord-ec9f388bfd9b4df79ccb6906c2ab361f
出典メモuspto-grants-1995_06