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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106003Generated: October 30, 2026

4-Nitrobenzyl alcohol → 4-NITROBENZYLFLUORIDE

https://huagongshe.com/reaction/1106003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl alcoholHCID 69275—
ReactantHCID 12797938HCID 12797938—
SolventDichloromethaneHCID 6344—
Product4-NITROBENZYLFLUORIDEHCID 1086656676.1%

Reaction Steps

A solution of 0.77 g (5 mmol) of 4-nitrobenzyl alcohol in 15 ml of methylene chloride was added dropwise over a period of 10 min to a stirred solution of 2.0 g (7.8 mmol) of 2,2,2-trifluoro-1-(trifluoromethyl)ethoxysulfur trifluoride in 5 ml of methylene chloride cooled to 10°. The reaction mixture was warmed to room temperature and then evaporated to dryness under reduced pressure. The residue was recrystallized from pentane to give 0.59 g (76% ) of 4-nitrobenzyl fluoride as colorless needles: mp 33° to 34°. Recrystallization from pentane raised the melting point to 36° to 37°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04311651
Source datasetuspto-grants-1982_01
ORD IDord-04f120749e404dbf8ab5d204c5c45d7f
Source noteuspto-grants-1982_01