Dimethylformamide → HCID 20338976, compound

HRID 1395345Notes

Reaction equation

[CH2:1]([O:3][C:4](=[O:28])[CH:5]([O:8][C:9]1[CH:14]=[C:13]([O:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][C:17]=2[Cl:26])[CH:12]=[CH:11][C:10]=1Br)[CH2:6][CH3:7])[CH3:2].[CH3:29][N:30](C)C=O>>[CH2:1]([O:3][C:4](=[O:28])[CH:5]([O:8][C:9]1[CH:14]=[C:13]([O:15][C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][C:17]=2[Cl:26])[CH:12]=[CH:11][C:10]=1[C:29]#[N:30])[CH2:6][CH3:7])[CH3:2]

Participants

Reactant 2

HCID 6228Dimethylformamide

HCID 20338977HCID 20338977, compound

Product 1

HCID 20338976HCID 20338976, compound

Procedure

A 10 g of ethyl-α-[2-bromo-5-(2-chloro-4-trifluoromethyl phenoxy)phenoxy]butyrate was dissolved in 20 ml of dimethylformamide.

Sources & evidence

ORD record: ord-403d2d3082ae43818eb156ce7938552b
Source dataset: uspto-grants-1980_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04203758

Reaction notes

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