Potassium Cyanide → 1,3-Dioxolane-2-propiononitrile

HRID 1955437Notes

Reaction equation

HRID 1955437 reaction equation
Br[CH2:2][CH2:3][CH:4]1[O:8][CH2:7][CH2:6][O:5]1.[C-:9]#[N:10].[K+]>CN(C)C=O.C1OCCOCCOCCOCCOCCOC1>[C:9]([CH2:2][CH2:3][CH:4]1[O:8][CH2:7][CH2:6][O:5]1)#[N:10]

Participants

5

Conditions

Temperature
23 °C

Procedure

A mixture of 2-(2-bromoethyl)-1,3-dioxolane (8.14 g, 45 mmol), potassium cyanide (5.85 g, 90 mmol), and 18-crown-6 (30 mg) in 30 mL of dimethylformamide was stirred for 72 hours at 23° C. The reaction mixture was filtered, diluted with 70 mL of dichloromethane and washed twice with 10 mL of water. The organic phase was dried over magnesium sulfate and distilled under vacuum to yield 3.2 g of 2-(2-cyanoethyl)-1,3-dioxolane. This was stirred in 20 mL of 1M HCl for 40 hours. The mixture was neutralized with sodium bicarbonate and extracted with 100 mL of dichloromethane. The dichloromethane extract was dried over magnesium sulfate and evaporated to yield 2.5 g of the desired aldehyde as an oil.

Workup

  1. filtrationThe reaction mixture was filtered
  2. additiondiluted with 70 mL of dichloromethane
  3. washwashed twice with 10 mL of water
  4. dry with materialThe organic phase was dried over magnesium sulfate
  5. distillationdistilled under vacuum

Sources & evidence

ORD record
ord-d6d2ca1aa8484f11a5649702007da728
Source dataset
uspto-grants-1998_07
Patent number
US05775329

Reaction notes

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