1-Iodo-4-(trifluoromethoxy)benzene → HCID 69461132, compound

HRID 852379Notes

Reaction equation

HRID 852379 reaction equation
[CH2:1]([O:3][C:4](=[O:21])[C:5]([O:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:16][CH2:17][C:18]#[CH:19])=[CH:11][C:10]=1[CH3:20])([CH3:7])[CH3:6])[CH3:2].I[C:23]1[CH:28]=[CH:27][C:26]([O:29][C:30]([F:33])([F:32])[F:31])=[CH:25][CH:24]=1>>[CH2:1]([O:3][C:4](=[O:21])[C:5]([CH3:6])([O:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:16][CH2:17][C:18]#[C:19][C:23]2[CH:24]=[CH:25][C:26]([O:29][C:30]([F:31])([F:32])[F:33])=[CH:27][CH:28]=2)=[CH:11][C:10]=1[CH3:20])[CH3:7])[CH3:2]

Participants

3

Procedure

In analogy to the procedure described in example 13B], 2-(4-but-3-ynyloxy-2-methyl-phenoxy)-2-methyl-propionic acid ethyl ester (example 16A]) and 1-iodo-4-trifluoromethoxy-benzene gave the title compound as a light yellow viscous oil.

Sources & evidence

ORD record
ord-9a689548ab354236920c4f5053e4a42e
Source dataset
uspto-grants-2007_08
Patent number
US07253192B2

Reaction notes

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