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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic acid, bromo-, diphenylmethyl ester → HCID 13603078, 화합물

HRID 2231980
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HRID 2231980 반응식
[OH:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.CC(C)([O-])C.[K+].Br[CH2:15][C:16]([O:18][CH:19]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17]>C1COCC1>[C:20]1([CH:19]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[O:18][C:16]([CH2:15][N:5]2[CH:6]=[CH:7][C:2](=[O:1])[CH:3]=[CH:4]2)=[O:17])[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11130534Acetic acid, bromo-, diphenylmethyl esterHCID 23665647Potassium tert-butoxideHCID 178418642HCID 178418642, 화합물

생성물 1

HCID 13603078HCID 13603078, 화합물수율 68.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

1.37 g of 4-hydroxypyridine was dissolved in 16 ml of THF, then 1.63 g of potassium tert-butoxide was added and reacted overnight. Thereafter, 3.12 g of diphenylmethyl bromoacetate was added and reacted for 6 hours. After the reaction, the solvent was removed, the residue was dissolved in chloroform and washed with water. This was dried over magnesium sulfate, the solvent was removed, and the residue was purified on silica gel chromatography using chloroform-methanol (20:1) to obtain 2.25 g of the title compound (55%).

후처리

  1. customreacted overnight
  2. customreacted for 6 hours
  3. customAfter the reaction
  4. customthe solvent was removed
  5. dissolutionthe residue was dissolved in chloroform
  6. washwashed with water
  7. dry with materialThis was dried over magnesium sulfate
  8. customthe solvent was removed
  9. customthe residue was purified on silica gel chromatography

출처 및 근거

ORD 기록
ord-8e8671beed454ee6a77e2b198e0281da
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04785090

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