Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076632Generated: October 31, 2026

Methyl (2-ethyl-4'-hydroxy-1,1'-biphenyl-4-yl)acetate → Methyl (2-ethyl-4'-{[2-formyl-3-hydroxy-4-(trifluoromethyl)benzyl]oxy}-1,1'-biphenyl-4-yl)acetate

https://huagongshe.com/reaction/2076632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl (2-ethyl-4'-hydroxy-1,1'-biphenyl-4-yl)acetateHCID 86088088—
Reactant2-(Dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)benzyl methanesulfonateHCID 86617407—
ProductMethyl (2-ethyl-4'-{[2-formyl-3-hydroxy-4-(trifluoromethyl)benzyl]oxy}-1,1'-biphenyl-4-yl)acetateHCID 8661740879%

Reaction Steps

According to a method similar to Example (40-2) and Example (8-3), from methyl (2-ethyl-4′-hydroxy-1,1′-biphenyl-4-yl)acetate (4.90 g, 18.1 mmol) obtained in Example (26-4) and 2-(dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)benzyl methanesulfonate (8.35 g, 21.5 mmol) obtained in Example (26-5), methyl (2-ethyl-4′-{[2-formyl-3-hydroxy-4-(trifluoromethyl)benzyl]oxy}-1,1′-biphenyl-4-yl)acetate was obtained as a colorless solid (6.77 g, two-step total yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923573B2
Source datasetuspto-grants-2011_04
ORD IDord-e28fd3303a564d379a1dc7a220a76786
Source noteuspto-grants-2011_04