Acetic Acid → HCID 86737671, compound

HRID 1065743Notes

Reaction equation

HRID 1065743 reaction equation
O.[CH:2](/[CH:7]1[CH:11]=[CH:10][CH2:9][C:8]1=[O:12])=[CH:3]/[CH2:4][CH2:5][CH3:6].C(O)(=O)C.[C-:17]#[N:18].[Na+]>C(O)C>[CH:2](/[CH:7]1[CH:11]([C:17]#[N:18])[CH2:10][CH2:9][C:8]1=[O:12])=[CH:3]/[CH2:4][CH2:5][CH3:6]

Participants

6

Conditions

Temperature
35 °C

Procedure

Into a 500 ml reaction flask equipped with mechanical stir, immersion thermometer, water cool bubble condenser, 150 ml addition funnel and heating mantle is placed 10 grams (0.07 moles) of 2-(2-cis-pentenyl)-3-cyclopenten-1-one prepared according to Example B; (0.07 moles); 4.20 grams of glacial acetic acid (0.07 moles) and 245 ml of 95% aqueous ethanol. The reaction mass is heated to 35° C. and, dropwise with stirring while keeping the temperature between 35° and 37° C., 6.86 grams (0.14 moles) of sodium cyanide (dissolved in 75 ml water) is added. After addition, the reaction mass is stirred at a temperature of 35° C. for a period of 3.5 hours.

Workup

  1. customInto a 500 ml reaction flask
  2. temperaturecool
  3. custombubble
  4. additioncondenser, 150 ml addition funnel
  5. temperatureheating mantle
  6. customprepared
  7. additionis added
  8. additionAfter addition
  9. stirringthe reaction mass is stirred at a temperature of 35° C. for a period of 3.5 hours

Sources & evidence

ORD record
ord-afb362e23f3c473d8b1bc06f682acc42
Source dataset
uspto-grants-1982_05
Patent number
US04331611

Reaction notes

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