Benzene → (3-Ethyl-2-hydroxyphenyl)(phenyl)methanone
Reaction equation
[CH:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:7][C:8]1[C:16]([CH2:17][CH3:18])=[CH:15][CH:14]=[CH:13][C:9]=1[C:10](Cl)=[O:11]>>[OH:7][C:8]1[C:16]([CH2:17][CH3:18])=[CH:15][CH:14]=[CH:13][C:9]=1[C:10]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)=[O:11]Participants
3
Procedure
This compound (44.67g) was prepared from benzene (172g.,2.2 mole) and 2-hydroxy-3-ethyl benzoic acid chloride (63.15g,0.34 mole), using the same conditions as in Example 30. The b.p. of the compound was 123°-126°C./0.14mm, ηD22 1.6081,νmax.(film) 1630cm-1.
Workup
- customwas 123°-126°C.
Sources & evidence
- ORD record
- ord-ffda8fb0273d4c46a235d9c7a3e268e0
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03951999
Reaction notes
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