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Pyrrolidine → HCID 54067199, 화합물

HRID 2418268
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인쇄 미리보기

반응식

HRID 2418268 반응식
[CH2:1]([C:6](=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Cl:17])[CH2:7]Br)[CH2:2][CH2:3][CH2:4][CH3:5].[NH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1>C(Cl)(Cl)Cl>[CH2:1]([C:6](=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][C:11]=1[Cl:17])[CH2:7][N:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1)[CH2:2][CH2:3][CH2:4][CH3:5]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31268PyrrolidineHCID 54161519HCID 54161519, 화합물

생성물 1

HCID 54067199HCID 54067199, 화합물수율 39.1%

시약·촉매·용매 1

HCID 6212Chloroform용매

반응 조건

온도
150 °C

실험 절차

A mixture of 50 g of (III) and 31.7 g of pyrrolidine was heated for 5 hours at 150° C. in an oil bath. The crude product was cooled, and dissolved in CHCl3, and the solution was washed with dilute NaOH and then several times with water. The organic phase was dried over Na2SO4 and concentrated. Distillation of the residue gave 19 g of (IV) of boiling point 148°-150° C./0.1 mbar.

후처리

  1. washthe solution was washed with dilute NaOH
  2. dry with materialThe organic phase was dried over Na2SO4
  3. concentrationconcentrated
  4. distillationDistillation of the residue

출처 및 근거

ORD 기록
ord-c0504e35b2d24b699831a131d498cb69
출처 데이터셋
uspto-grants-1984_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04472412

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