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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627725Generated: November 2, 2026

Sodium Hydroxide → 5-Chloro-2-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1627725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium HypochloriteHCID 23665760—
Reactant2-Hydrazino-3-chloro-6-trifluoromethyl pyridineHCID 69021031—
SolventDichloromethaneHCID 6344—
Product5-Chloro-2-(trifluoromethyl)pyridineHCID 13532658271.8%

Reaction Steps

19.91 g of 2-hydrazino-3-chloro-6-trifluoromethyl pyridine from the small batch and 30.19 g from the large batch were combined (50.10 g total, 0.237 mol) in a 2 L, three-neck flask with a mechanical stirrer and an addition funnel. Dichloromethane (190 g) and sodium hydroxide (237 g, 1N solution) were added to the flask. Sodium hypochlorite (NaOCl) (354 g, 0.238 mol, 5% solution) was charged to the addition funnel. The sodium hypochlorite solution was added over 1 hour as the solution turned yellow, then orange, and then purple-brown. The conversion was approximately 36% at the end of the sodium hypochlorite addition. The solution was stirred for an additional 6.5 hours, at which point the conversion was about 98%. Agitation was stopped and the solution was left overnight. The next morning, sodium hypochlorite (9 g, 0.006 mol, 5% solution) was added, and the solution was stirred for 1.5 hours, at which point sampling indicated that there was less than 1% starting material. The layers were separated and the aqueous layer was extracted twice with dichloromethane (100 mL). The organic layers were combined, washed with water, dried with magnesium sulfate, filtered, and concentrated on the rotovap to give 46.44 g of crude 3-chloro-6-trifluoromethyl pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785650B2
Source datasetuspto-grants-2014_07
ORD IDord-6bf84afe374640b2883c2913e5498b89
Source noteuspto-grants-2014_07