4-Fluorobenzaldehyde → HCID 69099855, compound

HRID 2252355Notes

Reaction equation

C(OP([CH2:9][C:10]1[CH:15]=[C:14]([O:16][CH3:17])[C:13]([CH:18]([CH3:20])[CH3:19])=[C:12]([O:21][CH3:22])[CH:11]=1)(=O)OCC)C.[F:23][C:24]1[CH:31]=[CH:30][C:27]([CH:28]=O)=[CH:26][CH:25]=1>>[CH3:17][O:16][C:14]1[CH:15]=[C:10]([CH:9]=[CH:28][C:27]2[CH:30]=[CH:31][C:24]([F:23])=[CH:25][CH:26]=2)[CH:11]=[C:12]([O:21][CH3:22])[C:13]=1[CH:18]([CH3:19])[CH3:20]

Participants

Reactant 2

HCID 680234-Fluorobenzaldehyde

HCID 46928247Diethyl (4-isopropyl-3,5-dimethoxybenzyl)phosphonate

Product 1

HCID 69099855HCID 69099855, compound

Procedure

This material was prepared from diethyl(3,5-dimethoxy-4-i-propylbenzyl)phosphonate and 4-fluorobenzaldehyde in the same procedure as described in example 21.

Sources & evidence

ORD record: ord-6cdbac6cf2234a6eb9d5d0c382dda08e
Source dataset: uspto-grants-2008_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07321050B2

Reaction notes

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