Formaldehyde → HCID 18176648, compound

HRID 1385997Notes

Reaction equation

HRID 1385997 reaction equation
[ClH:1].[F:2][C:3]([F:24])([F:23])[C:4]1[CH:5]=[C:6]([CH:20]=[CH:21][CH:22]=1)[O:7][CH2:8][CH2:9][CH2:10][CH2:11][NH:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C=O.S1C=CC=[CH:28]1.C([O-])(=O)C.[K+].[H][H]>CO.[Pd]>[ClH:1].[CH3:28][N:12]([CH2:11][CH2:10][CH2:9][CH2:8][O:7][C:6]1[CH:20]=[CH:21][CH:22]=[C:4]([C:3]([F:23])([F:24])[F:2])[CH:5]=1)[CH2:13][C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1

Participants

8

Procedure

A mixture of intermediate 7 (0.03 mol) and paraformaldehyde (2 g) in methanol (150 ml) was hydrogenated with palladium on carbon (2 g) as a catalyst in the presence of thiophene (4%, 2 ml) and potassium acetate (4 g). After uptake of hydrogen gas (1 equivalent), the catalyst was filtered off and the filtrate was evaporated. The residue was stirred in water and this mixture was extracted with DCM. The separated organic layer was dried, filtered, and the solvent evaporated. The residue was dissolved in DIPE and converted into the hydrochloric acid salt (1:1) with HCl/2-propanol. The precipitate was filtered off and dried, yielding 8.22 g (73%) of N-methyl-N-[4-[3-(trifluoro-methyl)phenoxy]butyl]benzenemethanamine hydrochloride (intermediate 8).

Workup

  1. customthe filtrate was evaporated
  2. extractionthis mixture was extracted with DCM
  3. customThe separated organic layer was dried
  4. filtrationfiltered
  5. customthe solvent evaporated
  6. dissolutionThe residue was dissolved in DIPE
  7. filtrationThe precipitate was filtered off
  8. customdried

Sources & evidence

ORD record
ord-721e8d182f42422b92f6d61e145a8f4c
Source dataset
uspto-grants-2001_07
Patent number
US06265407B1

Reaction notes

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