Pyridine → N-propyl-N-propoxy-bromoacetamide

HRID 902233Notes

Reaction equation

HRID 902233 reaction equation
Cl.[CH2:2]([NH:5][O:6][CH2:7][CH2:8][CH3:9])[CH2:3][CH3:4].N1C=CC=CC=1.[Br:16][CH2:17][C:18](Br)=[O:19]>C(#N)C>[CH2:2]([N:5]([O:6][CH2:7][CH2:8][CH3:9])[C:18](=[O:19])[CH2:17][Br:16])[CH2:3][CH3:4]

Participants

5

Conditions

Temperature
-20 °C

Procedure

N-Propyl-N-propoxyamine hydrochloride (0.30 g) was dissolved in acetonitrile and cooled to −20° C. Pyridine (0.2 mL) was added. Bromoacetyl bromide (0.15 g) was added dropwise over 5 min. The solution was stirred at −20° C. for 30 min. The bath was removed and the solution was stirred for 6 hours at room temperature. The solvent was removed in vacuo and the residue taken up in EtOAc (50 mL) and washed with water (1×25 mL), 1N phosphoric acid (3×25 mL), and brine (1×25 mL). The organic layer was dried with sodium sulfate and evaporated to give a dark orange oil (0.35 g). The product is a mixture of chloro- and bromoacetamides in a ratio of ˜3:1.

Workup

  1. customThe bath was removed
  2. stirringthe solution was stirred for 6 hours at room temperature
  3. customThe solvent was removed in vacuo
  4. washwashed with water (1×25 mL), 1N phosphoric acid (3×25 mL), and brine (1×25 mL)
  5. dry with materialThe organic layer was dried with sodium sulfate
  6. customevaporated

Sources & evidence

ORD record
ord-d0547400d0eb4071a58bf9ea759b6596
Source dataset
uspto-grants-2008_04
Patent number
US07365093B2

Reaction notes

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