Dichloromethane → 1-(Tert-butyldiphenylsilyloxymethyl)-2,6-dichloro-3-(phthalimidoacetylamino)benzene

HRID 2287550Notes

Reaction equation

HRID 2287550 reaction equation
[NH2:1][C:2]1[C:3]([Cl:28])=[C:4]([CH2:9][O:10][Si:11]([C:24]([CH3:27])([CH3:26])[CH3:25])([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[C:5]([Cl:8])=[CH:6][CH:7]=1.ClCCl.[C:32]1(=[O:46])[N:36]([CH2:37][C:38](Cl)=[O:39])[C:35](=[O:41])[C:34]2=[CH:42][CH:43]=[CH:44][CH:45]=[C:33]12>O>[Si:11]([O:10][CH2:9][C:4]1[C:5]([Cl:8])=[CH:6][CH:7]=[C:2]([NH:1][C:38](=[O:39])[CH2:37][N:36]2[C:35](=[O:41])[C:34]3=[CH:42][CH:43]=[CH:44][CH:45]=[C:33]3[C:32]2=[O:46])[C:3]=1[Cl:28])([C:24]([CH3:25])([CH3:27])[CH3:26])([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1

Participants

5

Procedure

To a mixture of 3-amino-1-(tert-butyldiphenylsilyloxy-methyl)-2,6-dichlorobenzene (348 mg) triethylamine (0.15 ml) and dichloromethane (3.5 ml) was added phthalimidoacetyl chloride (186 mg) under ice-cooling, and the mixture was stirred for 1.5 hours at ambient temperature. Water was added thereto, and the resulting precipitates were collected by vacuum filtration and washed with diisopropyl ether to give 1-(tert-butyldiphenylsilyloxymethyl)-2,6-dichloro-3-(phthalimidoacetylamino)benzene (460 mg) as crystals.

Workup

  1. temperaturecooling
  2. customthe resulting precipitates
  3. filtrationwere collected by vacuum filtration
  4. washwashed with diisopropyl ether

Sources & evidence

ORD record
ord-74c2cfb2b3144836bfec574e3dfc0932
Source dataset
uspto-grants-2000_07
Patent number
US06083961

Reaction notes

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