Hydrochloric Acid → S-(4-Methylbenzyl)-L-Cysteine t-Butyl Ester
Reaction equation
[CH3:1][C:2](=[CH2:4])[CH3:3].[CH3:5][C:6]1[CH:19]=[CH:18][C:9]([CH2:10][S:11][CH2:12][C@@H:13]([C:15]([OH:17])=[O:16])[NH2:14])=[CH:8][CH:7]=1.OS(O)(=O)=O.[OH-].[Na+].Cl>O1CCOCC1.CCOCC>[C:2]([O:17][C:15](=[O:16])[C@H:13]([CH2:12][S:11][CH2:10][C:9]1[CH:8]=[CH:7][C:6]([CH3:5])=[CH:19][CH:18]=1)[NH2:14])([CH3:3])([CH3:1])[CH3:4]Participants
8
Procedure
To a cold solution of isobutylene (50 ml) in dioxane (80 ml), add S-(4-methylbenzyl)-L-cysteine (5.0 g) and concentrated H2SO4 (10 ml). Seal the vessel, allow to warm to room temperature, and stir for 18 hr. Pour into 5% NaOH (500 ml), extract with Et2O (3×400 ml), dry (MgSO4) and concentrate the Et2O in vacuo to give an oil. Treat the oil with HCl in Et2O to give the title compound, white needles (2.76 g) m.p. 218° (dec).
Workup
- customSeal the vessel
- extractionextract with Et2O (3×400 ml)
- dry with materialdry (MgSO4)
- concentrationconcentrate the Et2O in vacuo
- customto give an oil
Sources & evidence
- ORD record
- ord-df1e9aa54ed6459587d78e86c0be590f
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05262436
Reaction notes
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