HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655207Generated: October 31, 2026
Methanol → 3,4-Dichloro-2-(hydroxymethyl)pyridine
https://huagongshe.com/reaction/1655207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3,4-Dichloro-2-methylpyridine | HCID 21922890 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4-Dichloro-2-(hydroxymethyl)pyridine | HCID 22117301 | — |
Reaction Steps
m-Chloroperbenzoic acid (32.63 g) in dichloromethane (400 ml) was added dropwise to a solution of 3,4 -dichloro-2 -picoline (25.53 g)in dichloromethane (100 ml) maintaining the temperature at 20°-25°. After standing for 16 hours at room temperature the solution was washed with 1 N NAOH, dried (K2CO3 ) and filtered to give a pale yellow solution. Trifluoroacetic anhydride (30 ml) was added dropwise to this solution maintaining the temperature at 15°-20°. After standing for 2 days at room temperature, methanol (100 ml) was added and the solution evaporated under reduced presure. The residue was treated with aqueous sodium carbonate and extracted into dichloromethane. After drying (K2CO3 ) and removal of solvent, the residue was recrystallised from pet. ether (60/80 ) to give 3,4 -dichloro-2 -hydroxymethylpyridine, 15.76 g, m.p. 66°-8°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250527 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-080221254b7f41feb105af8a698e71e2 |
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| Source note | uspto-grants-1993_10 |
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