Benzyl chloroformate → HCID 19753252, compound

HRID 373724Notes

Reaction equation

HRID 373724 reaction equation
C(=O)(O)[O-].[Na+].[NH2:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[CH2:12][CH2:11][CH2:10]2.[CH2:16]([O:23][C:24](Cl)=[O:25])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.S([O-])(O)(=O)=O.[Na+]>CC(C)=O.O.C(OCC)(=O)C>[C:24]([NH:6][C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[CH2:12][CH2:11][CH2:10]2)([O:23][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:25]

Participants

8

Procedure

Sodium bicarbonate (7.20 g) is added to a solution of 5-aminoindan (XVA, 5.71 g) in acetone (60 ml) and water (30 ml) 0°, followed by the dropwise addition of benzylchloroformate (6.8 ml, 8.07 g) over 5 min. The mixture is stirred at 0° for about 1 hr, then at 20-°25° overnight. The mixture is poured into aqueous sodium hydrogen sulfate (10%, 200 ml), and ethyl acetate (300 ml). The organic extract is washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated under reduced pressure is give an oil. The oil is purified by column chromatography on 60-200μ silica gel, eluting with ethyl acetate/hexane (10/90). The appropriate fractions are pooled and concentrated to give the title compound, mp 56°-59°; NMR (CDCl3, 300 MHz) 7.40-7.03, 7.11 7.05, 6.65, 5.18, 2.85 and 2.05 δ; IR (mineral oil mull) 3275, 2925, 1693.5, 1544 and 1236 cm-1 ; MS (m/e) 267, 223, 222 and 91.

Workup

  1. customat 20-°25°
  2. customovernight
  3. extractionThe organic extract
  4. washis washed with saturated aqueous sodium bicarbonate
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customis give an oil
  8. customThe oil is purified by column chromatography on 60-200μ silica gel
  9. washeluting with ethyl acetate/hexane (10/90)
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-0a782b72727043659b9a0e73ade6faca
Source dataset
uspto-grants-1992_11
Patent number
US05164510

Reaction notes

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