Hydrochloric Acid → HCID 10814767, compound
Reaction equation
[Si:1]([O:18][CH2:19][C:20]1[C:21]([CH3:34])=[C:22]([C:27]2[CH:31]=[CH:30][S:29][C:28]=2[C:32]#[N:33])[CH:23]=[CH:24][C:25]=1[CH3:26])([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>>[NH2:33][CH2:32][C:28]1[S:29][CH:30]=[CH:31][C:27]=1[C:22]1[CH:23]=[CH:24][C:25]([CH3:26])=[C:20]([CH2:19][O:18][Si:1]([C:14]([CH3:16])([CH3:15])[CH3:17])([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:21]=1[CH3:34]Participants
Conditions
- Temperature
- 0 °C
Procedure
A mixture of 3-(3-tert-butyldiphenylsilyloxymethyl-2,4-dimethylphenyl)-2-cyanothiophene (471 mg) and 1M borane-tetrahydrofuran complex (3 ml) was stirred for 30 minutes at 0° C. under nitrogen atmosphere and allowed to stand at ambient temperature overnight. To the mixture was added 4N hydrochloric acid (1.5 ml) under ice-cooling, and the mixture was stirred for 1 hour. The mixture was partitioned between ethyl acetate and water, and the separated organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform:methanol=50:1, V/V) to give 2-aminomethyl-3-(3-tert-butyldiphenylsilyloxymethyl-2,4-dimethylphenyl)thiophene (415 mg) as oil.
Workup
- waitto stand at ambient temperature overnight
- temperaturecooling
- stirringthe mixture was stirred for 1 hour
- customThe mixture was partitioned between ethyl acetate and water
- washthe separated organic layer was washed with water and brine
- dry with materialdried over magnesium sulfate
- customevaporated in vacuo
- customThe residue was purified by silica gel column chromatography (chloroform:methanol=50:1, V/V)
Sources & evidence
- ORD record
- ord-8dd4fca4460945538c7565d41195cee2
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06127389
Reaction notes
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