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Dichloromethane → N-methoxymethyl-N-methylpyrrolidinium bis(pentafluoroethanesulfonyl)imide

HRID 403082
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HRID 403082 반응식
[Cl-].[CH3:2][O:3][CH2:4][N+:5]1([CH3:10])[CH2:9][CH2:8][CH2:7][CH2:6]1.[N-:11]([S:22]([C:25]([C:28]([F:31])([F:30])[F:29])([F:27])[F:26])(=[O:24])=[O:23])[S:12]([C:15]([C:18]([F:21])([F:20])[F:19])([F:17])[F:16])(=[O:14])=[O:13].[Li+].ClCCl>O>[N-:11]([S:12]([C:15]([C:18]([F:21])([F:19])[F:20])([F:16])[F:17])(=[O:13])=[O:14])[S:22]([C:25]([C:28]([F:31])([F:30])[F:29])([F:27])[F:26])(=[O:24])=[O:23].[CH3:2][O:3][CH2:4][N+:5]1([CH3:10])[CH2:9][CH2:8][CH2:7][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 12096715Ethanesulfonamide, 1,1,2,2,2-pentafluoro-N-((1,1,2,2,2-pentafluoroethyl)sulfonyl)-, lithium salt (1:1)HCID 23116042N-methoxymethyl-N-methylpyrrolidinium chloride

생성물 1

HCID 131728535N-methoxymethyl-N-methylpyrrolidinium bis(pentafluoroethanesulfonyl)imide

시약·촉매·용매 1

HCID 962Water
용매

실험 절차

A 15.0 g quantity of N-methoxymethyl-N-methylpyrrolidinium chloride prepared in Example 10 was dissolved in 50 g of water, and 35.1 g of lithium bis(pentafluoroethanesulfonyl)imide was added to the solution. The mixture was stirred for 30 minutes, and dichloromethane was thereafter added to the mixture, followed by extraction. The organic layer was washed with 50 g of water ten times and then dried, giving 31.4 g of a colorless liquid as the desired product.

후처리

  1. extractionfollowed by extraction
  2. washThe organic layer was washed with 50 g of water ten times
  3. customdried

출처 및 근거

ORD 기록
ord-b64d33338b964fff85e844dc54de0474
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08747690B2

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