Acetic Acid → HCID 86737671, compound
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
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- customInto a 500 ml reaction flask
- temperaturecool
- custombubble
- additioncondenser, 150 ml addition funnel
- temperatureheating mantle
- customprepared
- additionis added
- additionAfter addition
- stirringthe reaction mass is stirred at a temperature of 35° C. for a period of 3.5 hours
Sources & evidence
- ORD record
- ord-808c498400a34a17a9a479528f27e394
- Source dataset
- uspto-grants-1981_10
- Patent number
- US04294863
Reaction notes
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