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3-Phenylprop-2-Enal → Cinnamyl Alcohol

HRID 1421359
Notes
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Reaction equation

HRID 1421359 reaction equation
[CH:1](=[O:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.CCCCCCCCCCCC>C(O)(C)C>[CH:7]1[CH:6]=[CH:5][C:4](/[CH:3]=[CH:2]/[CH2:1][OH:10])=[CH:9][CH:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 3073-Phenylprop-2-Enal2×HCID 8182Dodecane

Product 1

HCID 5315892Cinnamyl Alcohol

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent2×

Procedure

In a three-necked flask provided with reflux condenser and magnetic stirrer, 0.5 g (3.8 mmol) of cinnamaldehyde (trans-3-phenyl-2-propanol) and 12 g of isopropyl alcohol (for a starting material/catalyst ratio=1:1) or 1.5 g (11.3 mmol) of cinnamaldehyde and 36 g of isopropyl alcohol (starting material/catalyst=3:1) were refluxed under argon with 0.5 g of catalyst and 1.5 g of dodecane (as GC standard). After the end of the reaction time, the reaction mixture was analyzed by gas chromatography and the yield was determined. The results are summarized in Table 2 below:

Workup

  1. customIn a three-necked flask provided
  2. temperaturewith reflux condenser and magnetic stirrer

Sources & evidence

ORD record
ord-b3fef801a55e43e4a4d8415454df9456
Source dataset
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06075145

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes