Triethylamine → HCID 54032578, compound
Reaction equation
[CH:1]1([CH2:7][O:8][C:9]([NH:11][C@H:12]([C:21](O)=[O:22])[CH2:13][C:14]2[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=2)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(Cl)(=O)OCC.C(N(CC)CC)C>O1CCCC1>[CH:1]1([CH2:7][O:8][C:9]([NH:11][C@H:12]([CH2:21][OH:22])[CH2:13][C:14]2[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=2)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In 30 ml of tetrahydrofuran, 3.2 g of N-(cyclohexylmethoxycarbonyl)-tyrosine was dissolved. To the solution were added 1.1 g of ethyl chlorocarbonate and 1.0 g of triethylamine while cooling with ice and stirring. After stirring the mixture for 10 minutes, the precipitate was removed by filtration. The filtrate was added to a suspension of 1.0 g of sodium borohydride and 10 ml of tetrahydrofuran cooled with ice. The mixture was stirred for two hours, then neutralized with hydrochloric acid and concentrated in vacuo. The residue was extracted with ethyl acetate and the extract was washed with water, dried and concentrated to dryness. The residue was crystallized from ethyl acetate-petroleum ether to give 2.3 g of N-(cyclohexylmethoxycarbonyl)-tyrosinol with a melting point of 121°-126° C.
Workup
- temperaturewhile cooling with ice
- stirringAfter stirring the mixture for 10 minutes
- customthe precipitate was removed by filtration
- additionThe filtrate was added to a suspension of 1.0 g of sodium borohydride and 10 ml of tetrahydrofuran
- temperaturecooled with ice
- stirringThe mixture was stirred for two hours
- concentrationconcentrated in vacuo
- extractionThe residue was extracted with ethyl acetate
- washthe extract was washed with water
- customdried
- concentrationconcentrated to dryness
- customThe residue was crystallized from ethyl acetate-petroleum ether
Sources & evidence
- ORD record
- ord-787f1ba88b6e4daab1db6592493d8bd5
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04025644
Reaction notes
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