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p-Chlorothiophenol → (4-Chlorophenyl)(2,5-difluorobenzyl)sulfane

HRID 1178860
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HRID 1178860 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([SH:8])=[CH:4][CH:3]=1.[OH-].[Na+].[F:11][C:12]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:13]=1[CH2:14]Br>O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:14][C:13]2[CH:16]=[C:17]([F:20])[CH:18]=[CH:19][C:12]=2[F:11])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7815p-ChlorothiophenolHCID 14798Sodium HydroxideHCID 5228302-(Bromomethyl)-1,4-difluorobenzene

생성물 1

HCID 16681304(4-Chlorophenyl)(2,5-difluorobenzyl)sulfane수율 99.6%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

4-Chlorothiophenol (253 g, 1.75 mol) was dissolved in industrial methylated spirits (1265 mL) and 2M sodium hydroxide solution (901 mL) was added, maintaining the temperature below 20° C. A solution of 2,5-difluorobenzyl bromide (355 g, 1.72 mol) in industrial methylated spirits (250 mL) was added dropwise to the thiolate solution, maintaining the temperature below 15° C. Upon completion of the reaction, water (1000 mL) was added. The resulting slurry was aged at 5° C. and then filtered. The cake was washed sequentially with cold industrial methylated spirits:water (40:60) and then water (500 mL). Drying in vacuo at ambient temperature furnished 2-[[(4-chlorophenyl)thio]methyl]-1,4-difluorobenzene (462.3 g, 99.6%). 1H NMR (CDCl3) 7.23 (4H, s), 6.69-6.86 (3H, m) and 4.04 (2H, s).

후처리

  1. temperaturemaintaining the temperature below 20° C
  2. temperaturemaintaining the temperature below 15° C
  3. additionwas added
  4. customwas aged at 5° C.
  5. filtrationfiltered
  6. washThe cake was washed sequentially with cold industrial methylated spirits:water (40:60)
  7. customDrying in vacuo at ambient temperature

출처 및 근거

ORD 기록
ord-0fa869292e9b45499f80c38d4dcf7c44
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07276637B2

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