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1,4-Butane sultone → HCID 178506954, 화합물

HRID 2180876
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HRID 2180876 반응식
[C:1]([S:14]([NH2:17])(=[O:16])=[O:15])([C:4]([C:7]([C:10]([F:13])([F:12])[F:11])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2].O[Li:19].O.CC(OC)(C)C.[CH2:27]1[CH2:34][O:33][S:30](=[O:32])(=[O:31])[CH2:29][CH2:28]1>COCCOC>[C:1]([S:14]([NH:17][CH2:34][CH2:27][CH2:28][CH2:29][S:30]([O:33][Li:19])(=[O:32])=[O:31])(=[O:16])=[O:15])([C:4]([C:7]([C:10]([F:13])([F:11])[F:12])([F:9])[F:8])([F:6])[F:5])([F:3])[F:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 154111,4-Butane sultoneHCID 15413tert-Butyl methyl etherHCID 168937Lithium hydroxide, monohydrateHCID 10958205Perfluorobutane sulfonamide

생성물 1

HCID 178506954HCID 178506954, 화합물수율 7%

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane
용매

실험 절차

C4F9SO2N(H)C4H8SO3Li was prepared essentially according to the procedure described in Preparation 3 replacing C4F9SO2NH(C2H4OH) with C4F9SO2NH2 (15.0 g; 0.05 moles), and the corresponding amounts of the following were used: LiOH—H2O (2.32 g; 0.055 moles), MTBE (100 mL), DME (100 mL), and 1,4-butanesultone (7.5 g; 0.055 moles). A waxy white solid was isolated (1.57 g; 7% yield).

후처리

  1. customA waxy white solid was isolated (1.57 g; 7% yield)

출처 및 근거

ORD 기록
ord-92efabfe14294b5291a1c7cc7273902f
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06890452B2

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