Formaldehyde → 1-(Hydroxymethyl)-cyclohexanecarboxaldehyde

HRID 435161Notes

Reaction equation

HRID 435161 reaction equation
[CH2:1]=[O:2].[CH:3]1([CH:9]=[O:10])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.[OH-].[Na+]>CO>[CH:9]([C:3]1([CH2:1][OH:2])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1)=[O:10]

Participants

5

Conditions

Temperature
0 °C

Procedure

Methanol is added to a suspension of 37% formaldehyde solution (69 ml.) and cyclohexanecarboxaldehyde (100 g.; 0.89 mole) to afford a homogeneous solution. The mixture is cooled to 0° C. and a sodium hydroxide solution (1 N; 67 ml.) is added with stirring over the course of 15 minutes. The mixture is allowed to warm to room temperature and is stirred at 25° C. overnight. The solution is then concentrated, diluted with water and extracted with ether. The ether extract is dried, evaporated in vacuo and the residual colorless liquid is distilled to afford 51% of 1-formyl-1-hydroxymethylcyclohexane (65 g.), b.p. 120°-125° C./0.90 mm.

Workup

  1. customto afford a homogeneous solution
  2. temperatureto warm to room temperature
  3. stirringis stirred at 25° C. overnight
  4. concentrationThe solution is then concentrated
  5. additiondiluted with water
  6. extractionextracted with ether
  7. extractionThe ether extract
  8. customis dried
  9. customevaporated in vacuo
  10. distillationthe residual colorless liquid is distilled

Sources & evidence

ORD record
ord-9ea4fb92a5b94004a6db006505006597
Source dataset
uspto-grants-1983_08
Patent number
US04400512

Reaction notes

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