Hydrochloric Acid → 3182-88-5

HRID 1601112Notes

Reaction equation

HRID 1601112 reaction equation
[CH2:1]([NH2:5])[CH:2]([CH3:4])[CH3:3].Br[CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9].C(N(CC)CC)C.[ClH:20]>C(OCC)C>[ClH:20].[CH2:1]([NH:5][CH2:7][C:8]([O:10][CH2:11][CH3:12])=[O:9])[CH:2]([CH3:4])[CH3:3]

Participants

6

Procedure

A mixture of isobutylamine (0.90 mL, 0.0091 mol), bromoacetic acid, ethyl ester (1.0 mL, 0.0090 mol), and triethylamine (1.28 mL, 0.00918 mol) in diethylether (15 mL) was stirred at room temperature for 24 hours. The resulting suspension was filtered off and washed with diethylether. The filtrate and washings were combined and rotary evaporated to an oil. The oil was chromatographed on silica gel (150 g, 230-400 mesh) eluting with dichloromethane-diethylether (19:1, 8×125 mL; 15:1, 7×125 mL; 10:1, 15×125 mL). Fractions containing product were combined and rotary evaporated to give an oil. The oil was dissolved in diethylether, concentrated hydrochloric acid (0.52 mL, 0.0063 mol HCl) was added, and the volatiles were rotary evaporated to give a white solid. The solid was dried in vacuo; yield 1.0 g (59%).

Workup

  1. filtrationThe resulting suspension was filtered off
  2. washwashed with diethylether
  3. customrotary evaporated to an oil
  4. customThe oil was chromatographed on silica gel (150 g, 230-400 mesh)
  5. washeluting with dichloromethane-diethylether (19:1, 8×125 mL; 15:1, 7×125 mL; 10:1, 15×125 mL)
  6. additionFractions containing product
  7. customrotary evaporated
  8. customto give an oil
  9. customthe volatiles were rotary evaporated
  10. customto give a white solid
  11. customThe solid was dried in vacuo

Sources & evidence

ORD record
ord-f66d2ec40faf4edbb671f1924444376d
Source dataset
uspto-grants-1999_11
Patent number
US05977141

Reaction notes

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