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

3-Carboxybenzaldehyde → 3-Hydroxy-2,2-dimethylbutanoic acid

HRID 2080306
노트
인쇄 미리보기

반응식

HRID 2080306 반응식
BrC1[CH:3]=[C:4]([CH:7]=[CH:8]C=1F)[CH2:5]N.C(C1C=C(C=CC=1)[C:16]([OH:18])=[O:17])=O.CC(C)N=C=NC(C)C.ClCCCl.CN(C=[O:39])C>>[CH3:8][CH:7]([OH:39])[C:4]([C:16]([OH:18])=[O:17])([CH3:5])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 120773-CarboxybenzaldehydeHCID 12734DiisopropylcarbodiimideHCID 2724902(3-Bromo-4-fluorophenyl)methanamineHCID 20184825Dce dmf

생성물 1

HCID 1529843-Hydroxy-2,2-dimethylbutanoic acid

실험 절차

To a mixture of above resin-bound 3-bromo-4-fluoro-benzylamine (200 mg, 1.15 mmol/g (theoretical loading), 0.23 mmol) in DCE/DMF (1:1, 8 mL) was added 3-formylbenzoic acid (350 mg, 2.3 mmol) and DIC (0.36 mL, 2.3 mmol). The mixture was shaken at rt for overnight and was then washed with DMF (20 mL×2), DCM (20 mL×2), MeOH (20 mL×2) and DCM (20 mL×2). The resulting resin was dried in vacuum oven at 20° C. for overnight to yield DMHB resin-bound N-[(3-bromo-4-fluorophenyl)methyl]-3-formylbenzamide (0.23 mmol). An analytical amount of the resin was cleaved with 50% of TFA in DCE for 10 min. The resulting solution was concentrated in vacuo and dissolved in 0.5 mL of CH3CN. MS (ESI): 336 [M+H]+.

후처리

  1. washwas then washed with DMF (20 mL×2), DCM (20 mL×2), MeOH (20 mL×2) and DCM (20 mL×2)
  2. customThe resulting resin was dried in vacuum oven at 20° C. for overnight

출처 및 근거

ORD 기록
ord-7d91d53f86e34493b5c32c99bbecd035
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932247B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트