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Heptafluorobutanol → HCID 14330157, 화합물

HRID 359606
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HRID 359606 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[CH2:7]Cl)([O-:3])=[O:2].[F:12][C:13]([F:23])([C:16]([F:22])([F:21])[C:17]([F:20])([F:19])[F:18])[CH2:14][OH:15].[OH-].[K+]>CN(C)C=O>[F:12][C:13]([F:23])([C:16]([F:21])([F:22])[C:17]([F:18])([F:19])[F:20])[CH2:14][O:15][CH2:7][C:6]1[CH:9]=[CH:10][CH:11]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 9776HeptafluorobutanolHCID 12078alpha-Chloro-m-nitrotolueneHCID 14797Potassium Hydroxide

생성물 1

HCID 14330157HCID 14330157, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

100.0 g (0.58 mol) of 3-nitrobenzyl chloride and 128.3 g (0.62 mol, 1.05 equivalents) of 2,2,3,3,4,4,4-heptafluorobutanol(purity: 96%) were dissolved in 300 ml of dimethylformamide. To the resultant mixture 49.0 g (0.88 mol, 1.5 equivalents) of KOH pellets were added while the mixture was being cooled in a water bath. The reaction temperature is elevated to 43° C. and thereafter gradually restored to room temperature, and the reaction was completed after 30 minutes.

후처리

  1. temperaturewas being cooled in a water bath
  2. customis elevated to 43° C.
  3. customgradually restored to room temperature

출처 및 근거

ORD 기록
ord-69fd71bbc8ab43219a0cf0f70eb11e20
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05001275

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