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Water → HCID 21264588, 화합물

HRID 567115
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HRID 567115 반응식
[CH3:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[O:4][CH2:5][C:6]1[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=1[C:8](Cl)=[O:9].[NH:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1.O>COC(C)(C)C>[CH3:1][C:2]1[CH:18]=[CH:17][CH:16]=[CH:15][C:3]=1[O:4][CH2:5][C:6]1[CH:14]=[CH:13][CH:12]=[CH:11][C:7]=1[C:8]([N:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1)=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 31268PyrrolidineHCID 156802362-[(2-Methylphenoxy)methyl]benzoyl chloride

생성물 1

HCID 21264588HCID 21264588, 화합물수율 84.6%

시약·촉매·용매 1

HCID 15413tert-Butyl methyl ether용매

실험 절차

At 20 to 30° C., 15.6 g (0.06 mol) of 2-(2-methylphenoxymethyl)benzoyl chloride (EP-A 493 711, page 22) are added dropwise to a solution of 8.53 g (0.12 mol) of pyrrolidine in 40 ml of t-butyl methyl ether. The mixture is admixed with water and the organic phase is separated off, dried over sodium sulphate and concentrated under reduced pressure. The residue crystallizes when stirred with diisopropyl ether. 15 g (84.6% of theory) of N-[2-(2-methylphenoxymethyl)-benzoyl]-pyrrolidine are obtained.

후처리

  1. customthe organic phase is separated off
  2. dry with materialdried over sodium sulphate
  3. concentrationconcentrated under reduced pressure
  4. customThe residue crystallizes when

출처 및 근거

ORD 기록
ord-1d8526c2c4be46d2bcb6f30e859a24be
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06177459B1

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