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Propane sultone → HCID 71692790, 화합물

HRID 1480503
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HRID 1480503 반응식
[CH3:1][C:2]1[C:10]([CH3:12])([CH3:11])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([S:13]([O-:16])(=[O:15])=[O:14])[CH:8]=2)[N:3]=1.[Na+:17].[CH2:18]1[CH2:24][S:21](=[O:23])(=[O:22])[O:20][CH2:19]1>>[CH3:1][C:2]1[C:10]([CH3:11])([CH3:12])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([S:13]([O-:16])(=[O:15])=[O:14])[CH:8]=2)[N+:3]=1[CH2:19][CH2:18][CH2:24][S:21]([O-:23])(=[O:22])=[O:20].[Na+:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 14264Propane sultoneHCID 23666128sodium 2,3,3-trimethyl-3H-indole-5-sulfonate

생성물 1

HCID 71692790HCID 71692790, 화합물수율 97.3%

반응 조건

온도
110 °C

실험 절차

A mixture of 14 g of sodium 2,3,3-trimethyl-3H-indole-5-sulfonate and 14 g 1,3-propanesultone in 100 mL dicholorobenzene was heated at 110° C. for 2 h. After it cooled down, the solvent is decanted. The resulting solid was then dissolved in 100 mL of acetonitrile, and 300 mL of ethyl acetate was added. The resulting sticky solid was again stirred in 300 mL of ethyl acetate to yield 20 g of the product.

후처리

  1. temperatureAfter it cooled down
custom
the solvent is decanted
  • dissolutionThe resulting solid was then dissolved in 100 mL of acetonitrile
  • addition300 mL of ethyl acetate was added
  • 출처 및 근거

    ORD 기록
    ord-a031dc4f377f421bac004707484ed21c
    출처 데이터셋
    uspto-grants-2016_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09408924B2

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