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2-Phenylethanol → Phenylacetaldehyde

HRID 27845
Notes
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Reaction equation

HRID 27845 reaction equation
[C:1]1([CH2:7][CH2:8][OH:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>[Ag].O>[C:1]1([CH2:7][CH:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 60542-Phenylethanol

Product 1

HCID 998PhenylacetaldehydeYield 67%

Reagents, catalysts & solvents 2

HCID 23954SilverCatalystHCID 962WaterSolvent

Procedure

The same installation as in Example 1 is used. A catalyst comprising 82 parts of silver crystals of particle sizes from 0.1 to 2.5 mm is introduced, as a homogeneous bed, into the reactor. The height of the catalyst bed is 30 mm. Using a similar method to Example 1, a mixture of 150 parts of 2-phenylethanol and 60 parts of water with 210 parts of air is passed per hour over the catalyst at 540° C. and 1.1 bar. The residence time is 0.07 second and the throughput 0.2 tonne/m2.h. 99 parts of phenylacetaldehyde (in the form of a 73 percent strength by weight organic phase) are obtained per hour, corresponding to a yield of 67% of theory. The conversion is 78 percent and the space-time yield is 5 grams of phenylacetaldehyde per cm3 of catalyst volume per hour.

Workup

  1. additionis introduced, as a homogeneous bed, into the reactor
  2. waitis passed per hour over the catalyst at 540° C.

Sources & evidence

ORD record
ord-b2a8411aac314ac2b525c7037d0c0abb
Source dataset
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04224254

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes