Methylamine → HCID 12027889, compound

HRID 1967892Notes

Reaction equation

HRID 1967892 reaction equation
[CH2:1]([O:3][CH:4]([O:13][CH2:14][CH3:15])[C:5]1[CH:12]=[CH:11][C:8]([CH:9]=O)=[CH:7][CH:6]=1)[CH3:2].[CH3:16][NH2:17].[BH4-].[Na+]>CO>[CH2:1]([O:3][CH:4]([O:13][CH2:14][CH3:15])[C:5]1[CH:12]=[CH:11][C:8]([CH2:9][NH:17][CH3:16])=[CH:7][CH:6]=1)[CH3:2]

Participants

5

Procedure

A mixture of 4-(diethoxymethyl)benzaldehyde (1.04 g, 5 mmol) and methylamine (27-32% solution in methanol, 2.3 g, 20 mmol) in methanol (20 mL) was stirred at room temperature for 40 mins. The mixture was cooled to 0° C., sodium borohydride (0.284 g, 7.5 mmol) was added portionwise. After the addition, the mixture was stirred at room temperature for 4 hr. Methanol was removed under reduced pressure. The residue was partitioned between water (50 mL) and ethyl acetate (50 mL). The organic layer was separated. The aqueous layer was extracted with ethyl acetate (50 mL×3). The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, and concentrated to give crude 1-(4-(diethoxymethyl)phenyl)-N-methylmethanamine (1.1 g) as a light yellow oil which was used in the next step without further purification. LC-MS (ESI) m/z: 224 (M+1)+.

Workup

  1. temperatureThe mixture was cooled to 0° C.
  2. additionAfter the addition
  3. stirringthe mixture was stirred at room temperature for 4 hr
  4. customMethanol was removed under reduced pressure
  5. customThe residue was partitioned between water (50 mL) and ethyl acetate (50 mL)
  6. customThe organic layer was separated
  7. extractionThe aqueous layer was extracted with ethyl acetate (50 mL×3)
  8. washThe combined organic layers were washed with brine
  9. dry with materialdried over anhydrous sodium sulfate
  10. concentrationconcentrated

Sources & evidence

ORD record
ord-92e6e8de9a3147a884d427b344f4745d
Source dataset
uspto-grants-2013_04
Patent number
US08420650B2

Reaction notes

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