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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680871Generated: October 30, 2026

Thionyl Chloride → HCID 23454861, compound

https://huagongshe.com/reaction/1680871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 23454838HCID 23454838—
SolventBenzeneHCID 241—
ProductHCID 23454861HCID 2345486174.9%

Reaction Steps

A mixture of 14.3 g of 1-(2,3,4-trimethoxyphenyl)-2-methyl-2-nitropropanol, 11.9 g of thionyl chloride and 150 ml of anhydrous benzene is refluxed for 3.5 hours. After the reaction, the reaction mixture is evaporated to remove solvent. The residue (yellow oil) is purified by silica gel chromatography (Solvent: n-hexane-ethyl acetate (10:1). 11.4 g of 1-(2,3,4-trimethoxyphenyl)-1-chloro-2-methyl-2-nitropropane are thereby obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04276304
Source datasetuspto-grants-1981_06
ORD IDord-2184a44bdcbb4a4baeb9ae7ae6f0c3a1
Source noteuspto-grants-1981_06