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1-(4-Chloro-2-hydroxyphenyl)ethanone → 1-[2-Hydroxy-4-chlorophenyl]-3-[4-carboxydimethylmethyloxyphenyl]prop-2-en-1-one

HRID 549463
Notes
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Reaction equation

HRID 549463 reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].C([O:14][C:15]([C:17]1[C:24]([CH3:25])=[CH:23][C:20]([CH:21]=O)=[C:19]([O:26][CH3:27])[C:18]=1[CH3:28])=[O:16])C>>[OH:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:11])[CH:10]=[CH:21][C:20]1[CH:23]=[C:24]([CH3:25])[C:17]([C:15]([OH:16])=[O:14])=[C:18]([CH3:28])[C:19]=1[O:26][CH3:27]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 10515131-(4-Chloro-2-hydroxyphenyl)ethanoneHCID 865999714-Ethyloxycarbonyidimethylmethyloxybenzaldehyde2×

Product 1

HCID 865999701-[2-Hydroxy-4-chlorophenyl]-3-[4-carboxydimethylmethyloxyphenyl]prop-2-en-1-one

Procedure

This compound was synthesized from 2′-hydroxy-4′-chloroacetophenone and 4-ethyloxycarbonyldimethylmethyloxybenzaldehyde (starting material 9) according to general method 2 described earlier.

Sources & evidence

ORD record
ord-fe85301bfbc34253b4b4cb0ddf511988
Source dataset
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07943661B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes