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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906919Generated: November 3, 2026

Thionyl Chloride → HCID 13826416, compound

https://huagongshe.com/reaction/1906919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 13826415HCID 13826415—
ProductHCID 13826416HCID 13826416—

Reaction Steps

(2,4,7-Trichloronaphthalen-1-yl)methanol (1.0 g, 3.8 mmoles) was added portionwise to thionyl chloride (10 ml) with cooling (ice bath). The reaction mixture was stirred at room temperature for 30 minutes and at reflux for 2 hours and then concentrated to dryness in vacuo. The oily residue was taken up in methylene chloride and the solution dried over MgSO4. The solution was filtered and concentrated in vacuo to give 1.0 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654363
Source datasetuspto-grants-1987_03
ORD IDord-e98f61805c684a1b8fd945bb0224af58
Source noteuspto-grants-1987_03