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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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O-Toluidine → 1-Tolyl-3-pyrroline

HRID 366870
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HRID 366870 반응식
[CH3:1]/[CH:2]=[CH:3]\[CH3:4].[NH2:5][C:6]1[C:7]([CH3:12])=[CH:8][CH:9]=[CH:10][CH:11]=1>C1(C)C=CC=CC=1>[C:7]1([CH3:12])[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=1[N:5]1[CH2:4][CH:3]=[CH:2][CH2:1]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7242O-ToluidineHCID 5287573cis-2-BUTENE

생성물 1

HCID 158773171-Tolyl-3-pyrroline수율 89.2%

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
50 °C

실험 절차

To a solution of 60.0 g of the cis-2-butene derivative solution prepared in Example 1 and 250 g of toluene in a round flask reactor, 171.7 g (1.6 mol) of toluidine was added dropwise with stirring for 30 min. at 50° C. After 2 hours of stirring, the crystallized solid was removed by filtration; 42.0 g of 35% HCl (aq) was added to the filtrate, and then excess benzylamine hydrochloride was removed by filtration or extraction. After the solvent was evaporated under reduced pressure, 56.8 g of 1-tolyl-3-pyrroline (yield 89.2%) was obtained.

후처리

  1. stirringAfter 2 hours of stirring
  2. customthe crystallized solid was removed by filtration
  3. addition42.0 g of 35% HCl (aq) was added to the filtrate
  4. customexcess benzylamine hydrochloride was removed by filtration or extraction
  5. customAfter the solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-f5b78b3fc8784131b379d94e83cdaf85
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06130338

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