Hydrochloric Acid → 2-chloro-5-nitrobenzenethiol

HRID 721968노트

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HRID 721968 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[S:11]C#N.[BH4-].[Na+].Cl>CN(C=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[SH:11]

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 1277678Thiocyanic acid, 2-chloro-5-nitrophenyl esterHCID 4311764Sodium borohydride

생성물 1

HCID 47130122-chloro-5-nitrobenzenethiol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 2-chloro-5-nitrophenyl thiocyanate (4.38 g, 20.4 mmole) in dry DMF (70 mL) under inert atmosphere, excess sodium borohydride (1.1 g) was added. The mixture was stirred for half hour and poured over crushed ice. The mixture was acidified with 1 N HCl and left at 0° C. for 1 hr. The precipitate were collected by filtration and redissolved in CH2Cl2. The organic layer was further washed with water and dried with MgSO4. The solvent was removed in vacuo to afford yellow crystals. The product was used in the next step without further purification. 1H NMR (300 MHz, d6-acetone) δ: 8.42 (d, 1H, J=2.7 Hz), 7.98 (dd, 1H, J=8.7, 2.7 Hz), 7.68 (d, 1H, J=8.7 Hz), 5.26 (bs, 1H). 13C NMR (75 MHz, d6-acetone) δ: 147.5, 137.9, 136.4, 131.2, 124.8, 121.7. HR-MS (EI): calcd. for C6H4ClNO2S 189.9646 [M+]. found 189.9646.

후처리

  1. additionpoured
  2. customover crushed ice
  3. waitleft at 0° C. for 1 hr
  4. filtrationThe precipitate were collected by filtration
  5. dissolutionredissolved in CH2Cl2
  6. washThe organic layer was further washed with water
  7. dry with materialdried with MgSO4
  8. customThe solvent was removed in vacuo
  9. customto afford yellow crystals
  10. customThe product was used in the next step without further purification

출처 및 근거

ORD 기록
ord-a9c9d947838a4f5faa171b075a624ff9
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07138075B2

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