4-Methoxybenzoic Acid → N,4-Dimethoxy-N-methylbenzamide

HRID 1798669Notes

Reaction equation

HRID 1798669 reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][CH:4]=1.CCN=C=NCCC[N:20]([CH3:22])C.C1C=CC2N(O)N=NC=2C=1.[CH3:33][O:34]CN.CCN(C(C)C)C(C)C>C(Cl)Cl.O>[CH3:33][O:34][N:20]([CH3:22])[C:7](=[O:9])[C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:11][CH:10]=1

Participants

8

Procedure

To a stirred solution of 4-methoxybenzoic acid (10.0 g, 65.70 mmol) in DCM (50 mL) were added EDCI (18.90 g, 98.60 mmol), HOBT (10.0 g, 65.70 mmol), N-methoxy methylamine (13.0 g, 131.40 mmol) and DIPEA (34.3 mL, 197.20 mmol) at RT under a nitrogen atmosphere. The reaction mixture was stirred at RT for 12 h. The reaction mixture was diluted with water and the aqueous layer was extracted with DCM (3×100 mL). The combined organic extracts were washed with water (2×100 mL), brine (2×50 mL), dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure to afford crude product. The crude material was purified by flash column chromatography using 20% ethyl acetate in hexane and silica gel (230-400 Mesh) to afford N,4-dimethoxy-N-methylbenzamide (11.0 g, 86%) as a colorless liquid.

Workup

  1. extractionthe aqueous layer was extracted with DCM (3×100 mL)
  2. washThe combined organic extracts were washed with water (2×100 mL), brine (2×50 mL)
  3. dry with materialdried over anhydrous Na2SO4
  4. filtrationfiltered
  5. customevaporated under reduced pressure
  6. customto afford crude product
  7. customThe crude material was purified by flash column chromatography

Sources & evidence

ORD record
ord-ea88ef0c3acc4614aa43a946dd92bfdc
Source dataset
uspto-grants-2013_01
Patent number
US08343973B2

Reaction notes

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