Hydrochloric Acid → 4,4-Dimethyl-4,5,6,7-tetrahydro-thieno[2,3-c]pyridine

HRID 1640245Notes

Reaction equation

HRID 1640245 reaction equation
[CH2:1]=[N:2][CH2:3][C:4]([CH3:11])([C:6]1[CH:10]=[CH:9][S:8][CH:7]=1)[CH3:5].Cl.[OH-].[Na+]>>[CH3:5][C:4]1([CH3:11])[CH2:3][NH:2][CH2:1][C:7]2[S:8][CH:9]=[CH:10][C:6]1=2

Participants

4

Procedure

6.0 g (36 mmol) methylene-(2-methyl-2-thiophene-3-yl-propyl)-amine, 11 mL (45 mmol) 4M HCl and 12 mL (0.14 mol) conc. HCl were stirred at RT over the weekend. The reaction mixture was made alkaline with a 4M sodium hydroxide solution. The precipitate formed was suction filtered, washed with water and dried. The substance was purified on Alox. The product-containing fractions were combined and concentrated to dryness by rotary evaporation.

Workup

  1. customThe precipitate formed
  2. filtrationfiltered
  3. washwashed with water
  4. customdried
  5. customThe substance was purified on Alox
  6. concentrationconcentrated to dryness by rotary evaporation

Sources & evidence

ORD record
ord-680f1953957e4f0990b5377da3a6efd8
Source dataset
uspto-grants-2012_02
Patent number
US08110575B2

Reaction notes

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