Benzyl chloroformate → Benzyl 3-acetyl-1H-indole-1-carboxylate

HRID 1249234Notes

Reaction equation

HRID 1249234 reaction equation
[H-].[Na+].[C:3]([C:6]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[NH:8][CH:7]=1)(=[O:5])[CH3:4].Cl[C:16]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17]>C1COCC1>[C:16]([N:8]1[C:9]2[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6]([C:3](=[O:5])[CH3:4])=[CH:7]1)([O:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)=[O:17]

Participants

5

Procedure

To a stirred slurry of sodium hydride (3.77 g, 50% in oil, 7.86 mmol, extracted with hexanes) in THF (30 ml) at 0° C. under nitrogen was added dropwise 3-acetyl indole (10.0 g, 62.9 mmol) in THF (15 ml). After warming to room temperature and stirring one hour, the mixture was cooled to 0° C. and benzyl chloroformate (8.97 ml, 62.9 mmol) was added dropwise. The reaction was allowed to warm to room temperature and stir overnight. The excess sodium hydride was destroyed at 0° C. with 40 ml H2O. The mixture was then extracted three times with CHCl3 (total volume 120 ml), dried with MgSO4, filtered and evaporated to an off-white solid. Recrystallization from hexanes afforded 15.85 g (86%) of product: mp 112°-113°;

Workup

  1. temperaturethe mixture was cooled to 0° C.
  2. temperatureto warm to room temperature
  3. stirringstir overnight
  4. customThe excess sodium hydride was destroyed at 0° C. with 40 ml H2O
  5. extractionThe mixture was then extracted three times with CHCl3 (total volume 120 ml)
  6. dry with materialdried with MgSO4
  7. filtrationfiltered
  8. customevaporated to an off-white solid
  9. customRecrystallization from hexanes

Sources & evidence

ORD record
ord-4d7d9e14b5b447a7a0f35676b1b1d6b7
Source dataset
uspto-grants-1986_12
Patent number
US04629794

Reaction notes

Loading…