Cerium(III) chloride → 4-Hydroxycyclohex-1-ene-1-carbonitrile

HRID 521199Notes

Reaction equation

HRID 521199 reaction equation
[O:1]=[C:2]1[CH2:7][CH2:6][C:5]([C:8]#[N:9])=[CH:4][CH2:3]1.[Cl-].[Ce+3].[Cl-].[Cl-].[BH4-].[Na+]>CO.O>[OH:1][CH:2]1[CH2:7][CH2:6][C:5]([C:8]#[N:9])=[CH:4][CH2:3]1

Participants

6

Reactant 3

HCID 24636Cerium(III) chlorideHCID 4311764Sodium borohydrideHCID 189737114-Oxocyclohex-1-ene-1-carbonitrile

Product 1

HCID 867293624-Hydroxycyclohex-1-ene-1-carbonitrile

Reagents, catalysts & solvents 2

HCID 887MethanolSolvent2×HCID 962WaterSolvent

Procedure

To a stirred solution of 4-oxocyclohex-1-ene-1-carbonitrile (170 mg, 1.40 mmol) in MeOH (2.3 mL) at −78° C. was added cerium (III) chloride (484 mg, 1.96 mmol) in MeOH (4.7 mL). The resulting mixture was allowed to stir for 5 minutes at −78° C. before NaBH4 (48 mg, 1.26 mmol) was added in one portion. The mixture was stirred for 20 minutes and then allowed to warm to ambient temperature. After being stirred for 30 minutes, the reaction mixture was diluted with water and extracted with diethyl ether (3×). The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo (23° C. water bath) to afford the title compound.

Workup

  1. additionwas added in one portion
  2. stirringAfter being stirred for 30 minutes
  3. extractionextracted with diethyl ether (3×)
  4. washThe combined organic extracts were washed with brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo (23° C. water bath)

Sources & evidence

ORD record
ord-419dd61cae4f4fa59c2c2483768aad5d
Source dataset
uspto-grants-2016_05
Patent number
US09328099B2

Reaction notes

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