Hydrochloric Acid → S-(4-Methylbenzyl)-L-Cysteine t-Butyl Ester

HRID 257534Notes

Reaction equation

HRID 257534 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

  1. customSeal the vessel
  2. extractionextract with Et2O (3×400 ml)
  3. dry with materialdry (MgSO4)
  4. concentrationconcentrate the Et2O in vacuo
  5. 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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