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Benzylamine → Pentan-2-YL 4-hydroxybenzoate

HRID 1492348
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인쇄 미리보기

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HRID 1492348 반응식
C([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]([O:13][CH:14]([CH3:18])[CH2:15][CH2:16][CH3:17])=[O:12])=[CH:7][CH:6]=1)(=O)C.C(N)C1C=CC=CC=1>C(O)C.C(Cl)(Cl)Cl>[OH:4][C:5]1[CH:6]=[CH:7][C:8]([C:11]([O:13][CH:14]([CH3:18])[CH2:15][CH2:16][CH3:17])=[O:12])=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 7504BenzylamineHCID 189501354-Acetoxy-l-(1-methylbutyloxycarbonyl)benzene

생성물 1

HCID 19365293Pentan-2-YL 4-hydroxybenzoate수율 96.1%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6212Chloroform용매

실험 절차

Two grams of the crude compound (2) was dissolved in 50 ml of ethanol and 4 g of benzylamine was added dropwise. The mixture was stirred at room temperature for 4 hours, then diluted with 500 ml of chloroform, washed with dilute hydrochloric acid and water in this order, and dried with magnesium sulfate. After the solvent was evaporated, the residue was subjected to isolation and purification by silica gel column chromatography to obtain 1.6 g of a final compound.

후처리

  1. washwashed with dilute hydrochloric acid and water in this order
  2. dry with materialdried with magnesium sulfate
  3. customAfter the solvent was evaporated
  4. customthe residue was subjected to isolation and purification by silica gel column chromatography

출처 및 근거

ORD 기록
ord-1d632962eec24eb9be4f8d0db8c50c8f
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374375

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