홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrochloric Acid → (2R)-2-amino-3-methylbutane-1,3-diol hydrochloride

HRID 549108
노트
인쇄 미리보기

반응식

HRID 549108 반응식
[OH:1][C:2]([C@H:5]1[CH2:9][O:8]C(C)(C)[N:6]1C(OC(C)(C)C)=O)([CH3:4])[CH3:3].[ClH:19]>C(O)C>[ClH:19].[NH2:6][C@@H:5]([C:2]([CH3:4])([OH:1])[CH3:3])[CH2:9][OH:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 11379920Tert-butyl (R)-4-(2-hydroxypropan-2-YL)-2,2-dimethyloxazolidine-3-carboxylate

생성물 1

HCID 18341280(2R)-2-amino-3-methylbutane-1,3-diol hydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
85 °C

실험 절차

tert-Butyl (4R)-4-(1-hydroxy-1-methylethyl)-2,2-dimethyl-1,3-oxazolidine-3-carboxylate (7.32 g, 27.8 mmol), prepared by the method of Joullie, Tetrahedron, 52, pp. 11673-11694, (1996), was dissolved in 20 mL of ethanol. A 4.3 M solution of hydrochloric acid in ethanol (15 mL) was then added and the reaction mixture was heated 85° C. After 2 hours, the solution was cooled and concentrated under reduced pressure. The resulting residue was concentrated with 2-propanol several times and then with Et2O to give crude (2R)-2-amino-3-methylbutane-1,3-diol hydrochloride (4.32 g) as a brown oil. This was used in the next reaction without further purification.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperaturethe solution was cooled
  2. concentrationconcentrated under reduced pressure
  3. concentrationThe resulting residue was concentrated with 2-propanol several times

출처 및 근거

ORD 기록
ord-a53cc28988f346cdbb89798dd50277b9
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07943609B2

반응 노트

불러오는 중…