Sulfuric Acid → HCID 86735403, compound
Reaction equation
[C:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)(=[O:3])[CH3:2].S(=O)(=O)(O)O.[CH3:15][C:16]1[CH:21]=C(C(C)(C)C)C(O)=[C:18](C(C)(C)C)[CH:17]=1.CC(=C)CCO>O.C1CCCCC1>[CH3:2][C:1]1([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)[CH2:15][CH:16]([CH3:21])[CH:17]=[CH:18][O:3]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 94 °C
Procedure
Into a one-liter three neck flask equipped with stirrer, condenser, Barrett Trap, thermometer, addition funnel and heating mantle is placed 288 gms (2.4 moles) of acetophenone, 150 ml cyclohexane, 1 g of concentrated sulfuric acid and 1 g of Ionol®. The resulting mixture is heated to reflux temperature (94° C.). Then 208 gms (2.4 moles) of 3-methyl-3-buten-1-ol is added, dropwise from the addition funnel, to the reaction mass with stirring while maintaining the reaction mass at reflux. Water of reaction formed is azeotroped over into the Barrett Trap. The reaction mass is heated for a period of 10 hours, during which time 24 ml water collected. At the end of the 10 hour period, the reaction is cooled to room temperature and 2 gms of a 50% sodium hydroxide solution are added. The reaction mass is then rushed over using a 2 inch splash column after adding thereto 10 gms Primol® and 0.1 gms Ionol®. Fractions collected and fractionation data for this rush over is as follows:
Workup
- customInto a one-liter three neck flask equipped with stirrer, condenser
- additionBarrett Trap, thermometer, addition funnel
- temperatureheating mantle
- temperatureThe resulting mixture is heated
- temperaturewhile maintaining the reaction mass
- temperatureat reflux
- customformed
- customis azeotroped over into the Barrett Trap
- temperatureThe reaction mass is heated for a period of 10 hours, during which time 24 ml water
- customcollected
- temperatureAt the end of the 10 hour period, the reaction is cooled to room temperature
- addition2 gms of a 50% sodium hydroxide solution are added
- additionafter adding
- customFractions collected
Sources & evidence
- ORD record
- ord-13dbfec4b7fb451789ddb3024efa2763
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04115406
Reaction notes
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