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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172825Generated: October 25, 2026

Hexane → [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol

https://huagongshe.com/reaction/1172825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantAmmonium ChlorideHCID 25517—
Reactant(2-Chloro-6-fluoro-3-methoxyphenyl)trimethylsilaneHCID 46941339—
Reactant4-(4-Chlorophenoxy)-2-propylbenzaldehydeHCID 57420143—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanolHCID 86622409—

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a solution of 2,2,6,6-tetramethylpiperidine (2.75 g, 10 mmol) in THF (50 mL) cooled at −75° C. was added a solution of n-butyllithium in hexane (1.6 M, 6.3 mL, 10 mmol). After 15 min, 4-fluoro-2-chloro-3-(trimethylsilyl)anisole (2.3 g, 10 mmol) was added and the solution was warmed gradually to −40° C. over a 2 h period. The solution was recooled to −75° C. and a solution of the aldehyde from Step 1 of Example 3 (1.4 g, 5.0 mmol) in THF (3 mL) was added quickly. The reaction mixture was stirred for 15 min., poured into a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate. After removal of the solvent, the residue was purified by chromatography on silica gel to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834036B2
Source datasetuspto-grants-2010_11
ORD IDord-8ab7dbe4dfac470a9b7aa4d9fdbe6be1
Source noteuspto-grants-2010_11