HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085992Generated: October 25, 2026
Thionyl Chloride → 2-Chloromethyl-3-triphenylmethylthiopyridine hydrochloride
https://huagongshe.com/reaction/2085992
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Hydroxymethyl-3-triphenylmethylthiopyridine | HCID 9908047 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloromethyl-3-triphenylmethylthiopyridine hydrochloride | HCID 9845969 | 111.7% |
Reaction Steps
A thick suspension of 2-hydroxymethyl-3-triphenylmethylthiopyridine (90.3 g, 235 mmol) in N,N-dimethylformamide (270 mL) in a flask equipped with efficient mechanical stirring was chilled to 2° C. Thionyl chloride (25.8 mL, 354 mmol) was added in 5 mL portions over the period of 1 h while maintaining a temperature below 10° C. After completing the addition the reaction mixture was allowed to reach room temperature and was stirred for 30 min. The precipitate was filtered, washed with ethyl acetate (500 mL) and dried to give 86.7 g (84%) 2-chloromethyl-3-triphenylmethylthiopyridine hydrochloride as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06723716B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-ed4386c655034ee58cd48866a7e3d073 |
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| Source note | uspto-grants-2004_04 |
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