Hydrochloric Acid → HCID 66781221, compound

HRID 1096748Notes

Reaction equation

HRID 1096748 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C@@:9]2([C:14]#N)[CH2:11][CH:10]2[CH2:12][OH:13])[CH:5]=[CH:6][C:7]=1[Cl:8].C([OH:18])C.[OH-].[Na+].Cl>ClCCl>[Cl:1][C:2]1[CH:3]=[C:4]([C@@:9]23[CH2:11][C@@H:10]2[CH2:12][O:13][C:14]3=[O:18])[CH:5]=[CH:6][C:7]=1[Cl:8]

Participants

6

Procedure

(1R)-1-(3,4-Dichloro-phenyl)-2-hydroxymethyl cyclopropanecarbonitrile (24 g, 9.9 mmol), ethanol (48 mL) and 25N sodium hydroxide solution (24 mL) were heated under reflux for 18 hours. The reaction is monitored by TLC (dichloromethane (100%)). The reaction mixture was cooled to room temperature and ice cold water (24 mL) was added to the reaction mass followed by concentrated hydrochloric acid drop wise to adjust the pH of the reaction mass to 1-2 and stirred for overnight at room temperature. The aqueous layer was extracted with dichloromethane (100 mL).The organic layer was washed with 3% sodium bicarbonate solution, dried over anhydrous sodium sulphate, filtered and evaporated under reduced pressure to yield 13 g (55%) of product. 1H NMR δ(300 MHz,CDCl3): 1.41-1.43 (1H,t,J=4.9 Hz), 1.58-1.63 (1H,dd,J=7.8,5.0 Hz), 2.56-2.59 (1H,m), 4.28-4.31 (1H, d, J=9.3 Hz), 4.44-4.48 (1H, dd, J=9.4, 4.6 Hz), 7.26-7.30 (1H,dd,J=8.4,2.1 Hz), 7.40-7.43 (1H,d,J=8.4 Hz) 7.52-7.53 (1H,d,J=2 Hz).

Workup

  1. temperatureunder reflux for 18 hours
  2. extractionThe aqueous layer was extracted with dichloromethane (100 mL).The organic layer
  3. washwas washed with 3% sodium bicarbonate solution
  4. dry with materialdried over anhydrous sodium sulphate
  5. filtrationfiltered
  6. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-5b2555f511954f6c89c732653cc39dc8
Source dataset
uspto-grants-2012_03
Patent number
US08138377B2

Reaction notes

Loading…