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4-Isopropylbenzyl chloride → 3-Chloro-4-(4'-isopropylbenzyloxy) phenylacetic acid

HRID 27603
Notes
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Reaction equation

HRID 27603 reaction equation
[CH:1]([C:4]1[CH:11]=[CH:10][C:7]([CH2:8]Cl)=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[Cl:12][C:13]1[CH:14]=[C:15]([CH2:20][C:21]([O:23]C)=[O:22])[CH:16]=[CH:17][C:18]=1[OH:19]>CO.O>[Cl:12][C:13]1[CH:14]=[C:15]([CH2:20][C:21]([OH:23])=[O:22])[CH:16]=[CH:17][C:18]=1[O:19][CH2:8][C:7]1[CH:10]=[CH:11][C:4]([CH:1]([CH3:3])[CH3:2])=[CH:5][CH:6]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 749164-Isopropylbenzyl chlorideHCID 92625Methyl 3-chloro-4-hydroxyphenylacetate

Product 1

HCID 510572333-Chloro-4-(4'-isopropylbenzyloxy) phenylacetic acid

Reagents, catalysts & solvents 1

HCID 22242641Methanol--water (1/1)Solvent

Procedure

3-chloro-4-(4'-isopropylbenzyloxy) phenylacetic acid was prepared in accordance with the procedure designated (f) above by reacting 4-isopropylbenzyl chloride with methyl 3-chloro-4-hydroxyphenylacetate. The resultant product evidenced a melting point of 146.5°-148° C. in a methanol-water 2:1 mixture.

Sources & evidence

ORD record
ord-2f92acfef37b4fc4a8710866b2b3d64a
Source dataset
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04221919

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes