Hydrochloric Acid → HCID 54243229, compound

HRID 1650944Notes

Reaction equation

HRID 1650944 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([C:13]#[N:14])[CH2:12][CH2:11][CH2:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8].Br[CH2:16][CH2:17][CH2:18][C:19]1[O:20][C:21]([CH3:24])=[CH:22][CH:23]=1.[Mg].[BH4-].[Na+].Cl>CCOCC.CC(O)C.O>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([CH:13]([NH2:14])[CH2:16][CH2:17][CH2:18][C:19]3[O:20][C:21]([CH3:24])=[CH:22][CH:23]=3)[CH2:12][CH2:11][CH2:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8]

Participants

9

Procedure

1-(3,4-Dichlorophenyl)cyclobutanecarbonitrile (8 g) was added to the Grignard reagent prepared by the reaction under argon of 2-(3-bromopropyl)-5-methylfuran (10 g) and magnesium (1.1 g) in ether (20 ml). The mixture was stirred for 16 hours at ambient temperature. A suspension of sodium borohydride (3 g) in propan-2-ol (100 ml) was added and the mixture heated under reflux for 4.75 hours and then allowed to cool. The mixture was added to water with cooling and excess 2N hydrochloric acid added. The aqueous acid layer was extracted with ether and the extract washed with 1N aqueous sodium hydroxide solution, dried and evaporated to yield 1-[1-(3,4-dichlorophenyl)cyclobutyl]-4-(5-methyl-2-furyl)butylamine.

Workup

  1. additionwas added
  2. temperaturethe mixture heated
  3. temperatureunder reflux for 4.75 hours
  4. temperatureto cool
  5. temperaturewith cooling
  6. extractionThe aqueous acid layer was extracted with ether
  7. washthe extract washed with 1N aqueous sodium hydroxide solution
  8. customdried
  9. customevaporated

Sources & evidence

ORD record
ord-2790915a471944839946c298a140fe64
Source dataset
uspto-grants-1990_05
Patent number
US04925879

Reaction notes

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