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

Hydrochloric Acid → HCID 58856346, 화합물

HRID 899464
노트
인쇄 미리보기

반응식

HRID 899464 반응식
[NH2:1][C:2]([CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)([CH:7]([F:9])[F:8])[C:3](OC)=[O:4].[BH4-].[Li+].Cl>C1COCC1>[NH2:1][C:2]([CH:7]([F:8])[F:9])([CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[CH2:3][OH:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 4148881Lithium borohydrideHCID 18987073Methyl 2-amino-2-benzyl-3,3-difluoropropanoate

생성물 1

HCID 58856346HCID 58856346, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
45 °C

실험 절차

To a solution of methyl 2-amino-2-benzyl-3,3-difluoropropanoate (0.11 g, 0.48 mmol) (for synthesis see: Bey et al, J. Org. Chem. 1979, 44, 2732-2742) in 6.8 mL THF was added lithium borohydride (2M in THF, 1.45 mL, 2.9 mmol) dropwise. The reaction was heated at reflux temperature for 2 h, quenched with MeOH and acetone and concentrated. Hydrochloric acid (1M, 14.5 mL, 14.5 mmol) was added, the mixture was heated to 45° C. for 1.5 h and concentrated. The reaction was made basic with saturated NaHCO3 and extracted with CHCl3. Drying and solvent evaporation gave 2-amino-2-(difluoromethyl)-3-phenylpropan-1-ol. 1H NMR (400 MHz, CDCl3) δ 7.35-7.24 (m, 5H), 5.67 (t, J=56.5 Hz, 1H), 3.56 (A of AB, d, J=11.0 Hz, 1H), 3.46 (B of AB, d, J=11.0 Hz, 1H), 2.89 (A of AB, d, J=13.6 Hz, 1H), 2.84 (B of AB, d, J=13.6, 1H).

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux temperature for 2 h
  3. customquenched with MeOH and acetone
  4. concentrationconcentrated
  5. concentrationconcentrated
  6. extractionextracted with CHCl3
  7. customDrying
  8. customsolvent evaporation

출처 및 근거

ORD 기록
ord-6bac172ddd114a04b741cc56f247b6d4
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07354942B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트