Phenethylamine → HCID 21459098, compound

HRID 725316Notes

Reaction equation

HRID 725316 reaction equation
[C:1]1([CH2:7][CH2:8][NH2:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)CC)C.[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[C:26]([N+:30]([O-:32])=[O:31])[C:27]=1[O:28][CH3:29])[C:22](Cl)=[O:23]>C(Cl)Cl>[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[C:26]([N+:30]([O-:32])=[O:31])[C:27]=1[O:28][CH3:29])[C:22]([NH:9][CH2:8][CH2:7][C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:23]

Participants

5

Reactant 3

HCID 1001PhenethylamineHCID 8471TriethylamineHCID 219286153,4-Dimethoxy-5-nitrobenzoyl chloride

Product 1

HCID 21459098HCID 21459098, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

A solution of 1.49 g of 2-phenylethylamine in 100 ml of methylene chloride is treated with 1.26 g of triethylamine. A solution of 3.0 g of 3,4-dimethoxy-5-nitrobenzoyl chloride in 100 ml of methylene chloride is added dropwise thereto while stirring, whereupon the mixture is stirred for a further 15 minutes. The organic phase is then extracted twice with 50 ml of ice-water each time, dried over sodium sulfate and evaporated in a water-jet vacuum. After recrystallization from methylene chloride/n-hexane there is obtained 3,4-dimethoxy-5-nitro-N-phenethylbenzamide in the form of pale beige needles of m.p. 121°-122°.

Workup

  1. stirringis stirred for a further 15 minutes
  2. extractionThe organic phase is then extracted twice with 50 ml of ice-water each time
  3. dry with materialdried over sodium sulfate
  4. customevaporated in a water-jet vacuum
  5. customAfter recrystallization from methylene chloride/n-hexane there

Sources & evidence

ORD record
ord-2c966d33e4e048bd882f813bac500ae7
Source dataset
uspto-grants-1998_01
Patent number
US05705703

Reaction notes

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