Chloroform → 4-[N-Carbobenzyloxy-14-(trimethylsilyl)tetradecylamino]benzoyl chloride
Reaction equation
[CH3:1][Si:2]([CH3:28])([CH3:27])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][NH:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]([OH:24])=O)=[CH:20][CH:19]=1.C(Cl)(Cl)[Cl:30].C(=O)([O-])[O-].[Na+].[Na+].[C:39](Cl)([O:41][CH2:42][C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)=[O:40]>O>[C:39]([N:17]([CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][Si:2]([CH3:1])([CH3:28])[CH3:27])[C:18]1[CH:19]=[CH:20][C:21]([C:22]([Cl:30])=[O:24])=[CH:25][CH:26]=1)([O:41][CH2:42][C:43]1[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=1)=[O:40]Participants
6
Conditions
- Temperature
- 40 °C
Procedure
To 15 g. 4-[14-(trimethylsilyl)tetradecylamino]benzoic acid in 200 ml. warm chloroform is added a solution of 15 g. of sodium carbonate in 150 ml. water. To the vigorously stirred solution is added 10 g. carbobenzyloxy chloride. After 2 hours stirring at 40° C., the layers are separated, washed three times with 1N hydrochloric acid, dried, and evaporated to an oil. The oil is dissolved in 300 ml. toluene, treated with 15 ml. thionyl chloride and the solution is refluxed for 5 hours. The solvents are evaporated and the residue is dissolved three times in toluene, and evaporated to a viscous, orange oil.
Workup
- additionTo the vigorously stirred solution is added 10 g
- customthe layers are separated
- washwashed three times with 1N hydrochloric acid
- customdried
- customevaporated to an oil
- dissolutionThe oil is dissolved in 300 ml
- additiontoluene, treated with 15 ml
- temperaturethionyl chloride and the solution is refluxed for 5 hours
- customThe solvents are evaporated
- dissolutionthe residue is dissolved three times in toluene
- customevaporated to a viscous, orange oil
Sources & evidence
- ORD record
- ord-83401ad4eb1045a0863c97ddac957543
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04670421
Reaction notes
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