Sodium hydride → HCID 19082966, compound

HRID 1489479Notes

Reaction equation

HRID 1489479 reaction equation
[C:1]([NH:8][CH:9]1[CH2:11][CH2:10]1)(OC(C)(C)C)=O.[CH2:12]([O:19][CH2:20][CH2:21]CBr)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[H-].[Na+].[Cl-:26].[NH4+]>CN(C=O)C>[ClH:26].[CH2:12]([O:19][CH2:20][CH2:21][CH2:1][NH:8][CH:9]1[CH2:10][CH2:11]1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Participants

6

Procedure

8.58 g of N-BOC-cyclopropylamine and 15 g of O-benzyl-3-bromo-1-propanol in 90 ml of DMF are treated at 0°-5° with 2.5 g of sodium hydride (55% in oil). The mixture is stirred at 0°-5° for 1 hour and at room temperature for 3 hours and then treated at 0°-5° with aqueous ammonium chloride solution. The mixture is partitioned in ether/water and the ether phases are washed with water, then dried and concentrated. After chromatography over silica gel with ether/hexane (1:4), the 11.5 g of product are stirred with 120 ml of 4.8 molar hydrochloric acid in dioxane. After concentration, the residue is crystallized in ether. The crystals are filtered and washod with ether. There are obtained 9.0 g of (3-benzyloxy-propyl)-cyclopropyl-amine hydrochloride, MS (EI): 206 (M+H).

Workup

  1. customThe mixture is partitioned in ether/water
  2. washthe ether phases are washed with water
  3. customdried
  4. concentrationconcentrated
  5. stirringAfter chromatography over silica gel with ether/hexane (1:4), the 11.5 g of product are stirred with 120 ml of 4.8 molar hydrochloric acid in dioxane
  6. concentrationAfter concentration
  7. customthe residue is crystallized in ether
  8. filtrationThe crystals are filtered

Sources & evidence

ORD record
ord-3704f8510eec41749cbf5c9f98bd6506
Source dataset
uspto-grants-1997_10
Patent number
US05677448

Reaction notes

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