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Trifluoromethane → [3-(3-Chloro-5-cyano-phenoxy)-4-ethyl-2-fluoro-phenyl]-acetic acid ethyl ester

HRID 559053
Notes
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Reaction equation

HRID 559053 reaction equation
[CH:1](F)(F)F.[CH2:5]([O:7][C:8](=[O:28])[CH2:9][C:10]1[CH:15]=[CH:14][C:13]([CH3:16])=[C:12]([O:17][C:18]2[CH:23]=[C:22]([C:24]#[N:25])[CH:21]=[C:20]([Cl:26])[CH:19]=2)[C:11]=1[F:27])[CH3:6].C([Zn]CC)C>>[CH2:5]([O:7][C:8](=[O:28])[CH2:9][C:10]1[CH:15]=[CH:14][C:13]([CH2:16][CH3:1])=[C:12]([O:17][C:18]2[CH:23]=[C:22]([C:24]#[N:25])[CH:21]=[C:20]([Cl:26])[CH:19]=2)[C:11]=1[F:27])[CH3:6]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 6373TrifluoromethaneHCID 66999330[3-(3-Chloro-5-cyano-phenoxy)-2-fluoro-4-methyl-phenyl]-acetic acid ethyl esterHCID 178418750HCID 178418750, compound

Product 1

HCID 11545030[3-(3-Chloro-5-cyano-phenoxy)-4-ethyl-2-fluoro-phenyl]-acetic acid ethyl ester

Procedure

[3-(3-Chloro-5-cyano-phenoxy)-4-ethyl-2-fluoro-phenyl]-acetic acid ethyl ester (R-32) was prepared from R-23 using the procedure described for R-31 except diethylzinc was used in place of dimethylzinc.

Sources & evidence

ORD record
ord-cf1d37963042450cb712e052b48cd9f3
Source dataset
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08063064B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes