돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225103생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(Hydroxymethyl)-4-methylpentanoic acid

https://huagongshe.com/reaction/225103

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물DiisopropylamineHCID 7912—
반응물Isocaproic acidHCID 12587—
반응물Lithium, mol. (Li2)HCID 139759—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-(Hydroxymethyl)-4-methylpentanoic acidHCID 1178934390.4%

반응 조건

온도-20 °C

반응 단계

Diisopropylamine (20.6 g) is dissolved in 80 ml of dry tetrahydrofuran. This solution is cooled to -30° C. n-Butyllithium (77 ml of 2.6 M in hexane) is added dropwise in a nitrogen atmosphere at a rate that maintains the reaction at -30° to -20° C. This solution is stirred at -20° C. for 30 minutes. Isocaproic acid (11.6 g) in 10 ml of tetrahydrofuran is added dropwise at -20° to -10° C., then stirred at -10° C. for 30 minutes. In a separate flask, paraformaldehyde (28 g) is heated to about 200° C. and the vapors are carried in a stream of nitrogen over the surface of the tetrahydrofuran solution of the dilithium salt of isocaproic acid. During this procedure the temperature is kept between -10° and +10° C. After all of the paraformaldehyde has vaporized the reaction mixture is cooled to 0° C. and 10% hydrochloric acid is added dropwise until the reaction mixture becomes acidic. Product is extracted with 2 portions of ether (400 ml each). The ether is dried with magnesium sulfate, filtered and concentrated in vacuo to yield 13.2 g of crude material. Product is vacuum distilled to yield 9.0 g, boiling point 135°-142° C./9 mm of Hg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04235885
출처 데이터셋uspto-grants-1980_11
ORD IDord-c053824ad7f04e57a2a5f2906ad45306
출처 메모uspto-grants-1980_11