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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-(2-hydroxyethyl)-N'-(2-benzyloxybenzyl)urea → N-(2-hydroxyethyl)-N'-(2-hydroxybenzyl)urea

HRID 615225
노트
인쇄 미리보기

반응식

HRID 615225 반응식
[OH:1][CH2:2][CH2:3][NH:4][C:5]([NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[O:15]CC1C=CC=CC=1)=[O:6]>CO.[Pd]>[OH:1][CH2:2][CH2:3][NH:4][C:5]([NH:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[OH:15])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 13754437N-(2-hydroxyethyl)-N'-(2-benzyloxybenzyl)urea

생성물 1

HCID 13754438N-(2-hydroxyethyl)-N'-(2-hydroxybenzyl)urea

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

59.6 g of N-(2-hydroxyethyl)-N'-(2-benzyloxybenzyl)-urea are dissolved in 600 ml of methanol and hydrogenated in the presence of 6 g of Pd/C-catalyst (5%). After 2 hours the hydrogenation ceases. The catalyst is suction-filtered, and the filtrate concentrated by evaporation in vacuo. The residue is recrystallised from 350 ml of ethyl acetate; the pure product melts at 100°-101°.

후처리

  1. filtrationThe catalyst is suction-filtered
  2. concentrationthe filtrate concentrated by evaporation in vacuo
  3. customThe residue is recrystallised from 350 ml of ethyl acetate

출처 및 근거

ORD 기록
ord-d1cfa1536c80498090b9440570f58620
출처 데이터셋
uspto-grants-1985_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04497813

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