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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087922Generated: October 31, 2026

Hydrochloric Acid → Sodium Hypochlorite

https://huagongshe.com/reaction/1087922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantChlorineHCID 24526—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 178418543HCID 178418543—
ReactantHCID 178517756HCID 178517756—
ProductSodium HypochloriteHCID 23665760—
ProductHCID 178524411HCID 178524411—

Reaction Steps

Sodium hypochlorite solution was prepared by first adding 35.41 kg (442.6 mole) of 50% sodium hydroxide solution to 44 kg of flaked ice in a jacketed vessel having external circulating coolant; then adding 61.6 kg more flaked ice and introducing 7.87 kg (110.9 mole) of chlorine below the surface, all with agitation. To the sodium hypochlorite solution was added, portionwise, 15.0 kg of 98% purity (105.7 mole) 2-hydroxynicotinic acid (solids). The reaction temperature rose to 35° C. during the addition of the solids. Coolant was removed from the jacket and the mixture was stirred overnight at room temperature. A sample was withdrawn and acidified with concentrated hydrochloric acid to give precipitate which when analyzed by 1HNMR showed 75:25 ratio of title compound to starting 2-hydroxynicotinic acid. A second solution of sodium hypochlorite prepared as above from 10.57 kg of 50% sodium hydroxide solution (132.1 mole), 29.1 kg of ice and 3.65 kg (51.5 mole) of chlorine was added to the reaction mixture and the mixture was stirred overnight. This time a sample precipitated with concentrated hydrochloric acid showed no starting 2-hydroxynicotinic acid was present. Sodium bisulfite, 208 g (2.0 mole) was added to decompose unreacted excess sodium hypochlorite. Seven liters of isopropyl alcohol was then added to reduce expected foaming in the next step. The reaction mixture was added slowly to 41.48 kg (34.9 liters, 419.3 mole) of concentrated hydrochloric acid using external cooling to keep the mixture at 15°-25° C. pH of the mixture was 1.0. The slurry was filtered and the filter cake was washed with about 20 liters of water followed by 7 liters of acetone. The crystals were dried at 100° F. to a water content of about 5%; then milled and redried at 120° F. to a water content of 0.4%. The amount of crystals obtained was 17.42 kg (95.6% yield). 1HNMR analysis as described in Example 3 showed a trace of 3,5-dichloro-2-hydroxypyridine was present.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960896
Source datasetuspto-grants-1990_10
ORD IDord-6cfd96253bbc4f7b9dc283b5f4bae973
Source noteuspto-grants-1990_10