Aniline → 351325-32-1

HRID 970895Notes

Reaction equation

HRID 970895 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:8][CH2:9][C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=1)[C:13](Cl)=[O:14]>C(Cl)Cl>[Cl:8][CH2:9][C:10]1[CH:11]=[C:12]([CH:16]=[CH:17][CH:18]=1)[C:13]([NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:14]

Participants

4

Procedure

To a stirred solution of aniline (0.4 mL, 4.30 mmol) in anhydrous CH2Cl2 (10 mL) was added 3-chloromethylbenzoyl chloride (360 mg, 1.90 mmol). The reaction mixture was allowed to stir at room temperature overnight. The solvent was removed under reduced pressure. Purification of the residue on strong acid ion exchange resin column (elution with methanol) afforded the title compound (400 mg, 86%) as a white solid.

Workup

  1. customThe solvent was removed under reduced pressure
  2. customPurification of the residue
  3. washon strong acid ion exchange resin column (elution with methanol)

Sources & evidence

ORD record
ord-f2591f22a1024d08a30a9b84aff9483d
Source dataset
uspto-grants-2007_12
Patent number
US07312234B2

Reaction notes

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