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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433607Generated: October 25, 2026

Thionyl Chloride → 3-Bromo-5-(chloromethyl)pyridine

https://huagongshe.com/reaction/433607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(5-Bromo-3-pyridinyl)methanolHCID 2784733—
SolventDiethyl EtherHCID 3283—
Product3-Bromo-5-(chloromethyl)pyridineHCID 1170125999%

Reaction Conditions

Temperature4 °C

Reaction Steps

To a cooled solution of thionylchloride (41 ml, 344 mmol) at 0° C. was added cautiously (highly exothermic) portionwise (5-bromo-pyridin-3-yl)-methanol (10 g, 44.5 mmol). After complete addition the mixture was heated to reflux for 1 h to complete the reaction. After cooling, ether (50 ml) was added and the mixture cooled to 4° C. The precipitated solid was filtered off and washed with cold ether then dried at 50° C. under vacuum for 2 h to afford the title compound (9.1 g, 84%) as a light yellow solid. MS: m/e=206.9 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667335B2
Source datasetuspto-grants-2003_12
ORD IDord-e8c1a2c5785749f182fbf880b869b40b
Source noteuspto-grants-2003_12