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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70818Generated: October 29, 2026

Sodium Hydroxide → HCID 68195302, compound

https://huagongshe.com/reaction/70818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(2-Chloronaphthalen-1-yl)-3-methylpyridineHCID 68195084—
SolventDichloromethaneHCID 6344—
ProductHCID 68195302HCID 68195302—

Reaction Conditions

Temperature0 °C

Reaction Steps

A round-bottomed flask having a volume of 50 mL and equipped with a glass stopper and a three-way cock was dried, and 890 mg (3.51 mmol) of 2-(2-chloronaphthalen-1-yl)-3-methylpyridine and 20 mL of dichloromethane were introduced thereinto. This colorless solution was cooled to 0° C., and then 1.59 g (69-75%) of m-CPBA (meta-chloroperbenzoic acid) was each added thereto three times at intervals of 10 minutes. Next, the temperature was slowly increased to room temperature, and the colorless solution was stirred for 2 hours. Thereafter, the solution was cooled to 0° C. again, and 10 mL of an aqueous NaOH solution having a concentration of 1M was gradually added. Thereafter, an organic layer was washed with 10 mL of an aqueous NaOH solution having a concentration of 1M and 10 mL of salt water, then dried with 50 g of sodium sulfate, and subjected to dehydration and filtration steps, thereby obtaining 947 mg of yellow oily 2-(2-chloronaphthalen-1-yl)-5-methylpyridine-1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822696B2
Source datasetuspto-grants-2014_09
ORD IDord-ccbb045796ad4830ad7db75f7ccfe1b5
Source noteuspto-grants-2014_09