Hydrochloric Acid → S-Biphenyl-3-yl O-ethyl carbonodithioate

HRID 522565

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HRID 522565 반응식
[C:1]1([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[C:3](N)[CH:2]=1.Cl.N([O-])=O.[Na+].[O:19]([CH2:23][CH3:24])[C:20]([S-:22])=[S:21].[K+]>O>[C:20]([S:22][C:3]1[CH:2]=[C:1]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=1)(=[S:21])[O:19][CH2:23][CH3:24]

참가 물질

6

실험 절차

To a solution of 1 equiv. of biphenyl-3-amine (1 g, 5.92 mmol) in water (7.3 mL) at 0° C. was added concentrated hydrochloric acid (1 mL). A cold solution of 1.1 equiv. of sodium nitrite (450 mg, 6.5 mmol) in water (3 mL) was added slowly and stirred for 15 min. The cold diazonium solution was added slowly to a solution of 1.3 equiv. of potassium ethyl xanthate (1.16 g, 1.3 mmol) in water (1.3 mL) at 45° C. The reaction mixture was stirred for an additional 30 min at 45° C. and then cooled to RT. The reaction mixture was extracted with diethyl ether (3×50 mL). The combined organic extracts were washed with 1 N NaOH solution (100 mL), water (3×50 mL), brine (50 mL), dried over MgSO4, filtered and evaporated under reduced pressure. The resulting crude xanthate 52a was used directly in the next step without further purification. MS (ESI) m/z 275.0 (M+H)+.

후처리

  1. stirringThe reaction mixture was stirred for an additional 30 min at 45° C.
  2. extractionThe reaction mixture was extracted with diethyl ether (3×50 mL)
  3. washThe combined organic extracts were washed with 1 N NaOH solution (100 mL), water (3×50 mL), brine (50 mL)
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated under reduced pressure
  7. customThe resulting crude xanthate 52a was used directly in the next step without further purification

출처 및 근거

ORD 기록
ord-c8bef21ac14747179ee61bc2cc6e25c7
출처 데이터셋
uspto-grants-2016_05
특허 번호
US09334242B2

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