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Hydrochloric Acid → 3,4-Difluorobenzyl Mercaptan

HRID 1455011
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HRID 1455011 반응식
N[C:2](N)=[S:3].[F:5][C:6]1[CH:7]=[C:8]([CH:11]=[CH:12][C:13]=1[F:14])CBr.Cl>C(O)C.[OH-].[Na+]>[F:5][C:6]1[CH:7]=[C:8]([CH2:2][SH:3])[CH:11]=[CH:12][C:13]=1[F:14]
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 5814364-(Bromomethyl)-1,2-difluorobenzeneHCID 2723790Thiourea

생성물 1

HCID 27614283,4-Difluorobenzyl Mercaptan

시약·촉매·용매 2

HCID 702Ethanol용매HCID 14798Sodium Hydroxide용매

실험 절차

Thiourea (5.0 g) was added to a solution of 3,4-difluorobenzyl bromide (13.6 g) in ethanol (100 ml). The mixture was heated at reflux for 3 h before removal of the volatiles in vacuo. The crude solid was suspended in aqueous sodium hydroxide solution (1.6M, 110 ml) and heated at reflux for 3 h before allowing to cool to room temperature. The reaction was acidified with concentrated hydrochloric acid and the organics extracted with ether (200 ml). The organic layer was washed with saturated sodium bicarbonate solution (2×50 ml), brine (20 ml), dried (MgSO4), and concentrated in vacuo to provide the subtitle product as a colourless oil. Yield 11.1 g

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 3 h before removal of the volatiles in vacuo
  3. temperatureheated
  4. temperatureat reflux for 3 h
  5. extractionthe organics extracted with ether (200 ml)
  6. washThe organic layer was washed with saturated sodium bicarbonate solution (2×50 ml), brine (20 ml)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-09df2e4c3698490e81152dac35327843
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482355B2

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