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Benzylamine → 2-Fluoro-4-hydroxy-1-(2-ethylbutyloxy)carbonylbenzene

HRID 1384038
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HRID 1384038 반응식
[F:1][C:2]1[CH:7]=[C:6]([O:8]C(=O)C)[CH:5]=[CH:4][C:3]=1[C:12]([O:14][CH2:15][CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[O:13].C(N)C1C=CC=CC=1>C(O)C.CCOCC>[F:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[C:12]([O:14][CH2:15][CH:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7504BenzylamineHCID 211854772-Fluoro-4-acetoxy-1-(2-ethylbutyloxy)carbonylbenzene

생성물 1

HCID 211854782-Fluoro-4-hydroxy-1-(2-ethylbutyloxy)carbonylbenzene수율 95%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 3283Diethyl Ether용매

실험 절차

9.3 Grams (0.036 mol) of the compound prepared in the above (1) was dissolved in 250 ml of ethanol, and 7.7 g (0.0772 mol) of benzylamine was dropwise added. Further, the mixture was stirred at room temperature for 1 day, then diluted with 300 ml of ether, consecutively washed with diluted hydrochloric acid and with water, and dried over magnesium sulfate. The solvent was distilled off, and the residue was purified for isolation with a silica gel column chromatograph to give an end product in the yield of 95%.

후처리

  1. washconsecutively washed with diluted hydrochloric acid and with water
  2. dry with materialdried over magnesium sulfate
  3. distillationThe solvent was distilled off
  4. customthe residue was purified for isolation with a silica gel column chromatograph
  5. customto give an end product in the yield of 95%

출처 및 근거

ORD 기록
ord-2064d2953a1e44c6ae35075e98f8d5a2
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06258296B1

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