Hydrochloric Acid → 1-Methyl-1H-pyrazole-4-propanal

HRID 2288224ノート

反応式

HRID 2288224 の反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH3:11][N:12]1[CH:16]=[C:15]([CH2:17][CH2:18][CH2:19][OH:20])[CH:14]=[N:13]1.Cl>ClCCl.C(N(CC)CC)C>[CH3:11][N:12]1[CH:16]=[C:15]([CH2:17][CH2:18][CH:19]=[O:20])[CH:14]=[N:13]1

参加物

7

実験手順

To a solution of oxalyl chloride (0.361 ml) in dichloromethane (10 ml) cooled below -65° C. with a dry ice-acetone bath, a solution of dimethyl sulfoxide (0.381 ml) in dichloromethane (1 ml) was added with efficient stirring over 10 minutes. After 20 minutes below -65° C., a solution of 3-(1-methyl-1H-pyrazol-4-yl)-1-propanol in dichloromethane (2 ml) was added to the mixture over 10 minutes below -65° C. and the mixture was stirred at the same temperature for 20 minutes and then at -45~-40° C. for 30 minutes. After addition of triethylamine dropwise to the mixture over 10 minutes followed by stirring for 15 minutes, 1N hydrochloric acid solution was added to the mixture. The resulting mixture was extracted with a mixture of dichloromethane and methanol several times. The extract was concentrated under reduced pressure and the resulting residue was chromatographed on a silica gel using a mixture of dichloromethane and methanol as an eluent to give 3-(1-methyl-1H-pyrazol-4-yl)-1-propanal.

後処理

  1. waitAfter 20 minutes below -65° C.
  2. stirringthe mixture was stirred at the same temperature for 20 minutes
  3. waitat -45~-40° C. for 30 minutes
  4. stirringby stirring for 15 minutes
  5. extractionThe resulting mixture was extracted with a mixture of dichloromethane and methanol several times
  6. concentrationThe extract was concentrated under reduced pressure
  7. customthe resulting residue was chromatographed on a silica gel using
  8. additiona mixture of dichloromethane and methanol as an eluent

出典と根拠

ORDレコード
ord-616633f52b5b42e9933a19d496424a5b
出典データセット
uspto-grants-2000_07
特許番号
US06087357

反応ノート

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