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Triethylamine → HCID 20397540, 화합물

HRID 462842
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HRID 462842 반응식
Cl[CH2:2][CH2:3][S:4]([CH2:7][CH2:8][C:9]([F:27])([F:26])[C:10]([F:25])([F:24])[C:11]([F:23])([F:22])[C:12]([F:21])([F:20])[C:13]([F:19])([F:18])[C:14]([F:17])([F:16])[F:15])(=[O:6])=[O:5].C(N(CC)CC)C>C1COCC1>[CH:3]([S:4]([CH2:7][CH2:8][C:9]([F:27])([F:26])[C:10]([F:24])([F:25])[C:11]([F:22])([F:23])[C:12]([F:20])([F:21])[C:13]([F:18])([F:19])[C:14]([F:15])([F:16])[F:17])(=[O:6])=[O:5])=[CH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8471TriethylamineHCID 203975378-(2-Chloroethanesulfonyl)-1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorooctane

생성물 1

HCID 20397540HCID 20397540, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

2-(Perfluorohexyl)ethanyl 2-chloroethanyl sulfone (4.75 g, 10.0 mmole) was dissolved in 25 ml of THF at 30°, and triethylamine (1.52 g, 15.0 mmole) in 10 ml of THF was added in one minute. A white precipitate formed, and was filtered (1.37 g). The solvent was stripped carefully, as some foaming occurred.

후처리

  1. customA white precipitate formed
  2. filtrationwas filtered (1.37 g)

출처 및 근거

ORD 기록
ord-c3683595c59f405c8c1c64c3c3bb343a
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04517384

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