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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Pentamethylsilylamine → Bis(dimethylamino)-N,N-dimethylmethaniminium methyl sulfate

HRID 2116864
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HRID 2116864 반응식
[CH3:1][N:2]([Si](C)(C)C)[CH3:3].[CH3:8][O:9][S:10]([O-:13])(=[O:12])=[O:11].[CH3:14][N:15]([C+:17]([N:19]([CH3:21])[CH3:20])Cl)[CH3:16]>C(Cl)(Cl)Cl>[CH3:1][N:2]([CH3:3])[C:17](=[N+:15]([CH3:16])[CH3:14])[N:19]([CH3:21])[CH3:20].[CH3:8][O:9][S:10]([O-:13])(=[O:12])=[O:11]
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참가 물질

4

반응물 2

HCID 74965PentamethylsilylamineHCID 178483689HCID 178483689, 화합물

생성물 1

HCID 13127877Bis(dimethylamino)-N,N-dimethylmethaniminium methyl sulfate수율 95.5%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

10 ml of dry chloroform and 1.29 g (11.00 mmol) of N,N-dimethyltrimethylsilylamine are added to 2.45 g (9.93 mmol) of bis(dimethylamino)chlorocarbenium methylsulfate. The reaction mixture is stirred for 1 hour at room temperature, and all volatile compounds are subsequently removed under reduced pressure. The residue is dried for a further 1 hour under reduced pressure at 7.0 Pa and an oil-bath temperature of 50° C., giving 2.42 g of hexamethylguanidinium methylsulfate, corresponding to a yield of 95.5%.

후처리

  1. customall volatile compounds are subsequently removed under reduced pressure
  2. customThe residue is dried for a further 1 hour under reduced pressure at 7.0 Pa and an oil-bath temperature of 50° C.

출처 및 근거

ORD 기록
ord-53f587e8cfe14d7ba855527992d01d50
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07439395B2

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