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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13348Generated: October 26, 2026

Chloroform → 1-(2-Fluoro-4-nitro-phenyl)-3-buten-1-ol

https://huagongshe.com/reaction/13348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAllyltrimethylsilaneHCID 69808—
Reactant2-Fluoro-4-nitrobenzaldehydeHCID 4562919—
CatalystTitanium TetrachlorideHCID 24193—
SolventEthyl AcetateHCID 8857—
Product1-(2-Fluoro-4-nitro-phenyl)-3-buten-1-olHCID 23145779—

Reaction Steps

0.65 ml of titanium tetrachloride was added to a chloroform (12 ml) solution of 2.00 g of 4-nitro-2-fluoro-benzaldehyde produced according to the method described in U.S. Pat. No. 6,239,152, and the reaction liquid was stirred at room temperature for 10 minutes, and then 2.4 ml of allyl-trimethyl-silane was added to it, and the reaction liquid was stirred at room temperature for 20 minutes. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=3/1) to obtain the entitled compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-e409d2c505314342bc35b68cf061a516
Source noteuspto-grants-2010_06