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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 1310729-90-8

HRID 1969574
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HRID 1969574 반응식
[F:1][C:2]1([F:10])[CH2:5][CH:4]([S:6]([O-])(=[O:8])=[O:7])[CH2:3]1.[K+].S(Cl)([Cl:14])=O>CN(C=O)C>[F:1][C:2]1([F:10])[CH2:5][CH:4]([S:6]([Cl:14])(=[O:8])=[O:7])[CH2:3]1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 86660435HCID 86660435, 화합물

생성물 1

HCID 585574261310729-90-8수율 100.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide촉매

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온도
60 °C

실험 절차

To a suspension of potassium 3,3-difluorocyclobutane-1-sulfonate (0.250 g, 1.189 mmol) in thionyl chloride (2.60 mL, 35.7 mmol) was added DMF (3 drops). The reaction was heated to about 60° C. for about 21 h. The solvent was removed under reduced pressure and the residue was used in the next reaction without further workup or purification to afford crude 3,3-difluorocyclobutane-1-sulfonyl chloride (0.227 g, 100%) as product. 1H NMR (400 MHz, CDCl3) δ 4.33-4.17 (m, 1H), 3.28 (dd, J=11.1, 7.6 Hz, 2H), 3.21-3.05 (m, 2H).

후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe residue was used in the next reaction without further workup or purification

출처 및 근거

ORD 기록
ord-ecf17945ccfa4220ab80ec8419e2f770
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08426411B2

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