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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419456Generated: October 31, 2026

Sulfuric Acid → alpha-Hydroxyacetophenone

https://huagongshe.com/reaction/2419456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetophenoneHCID 7410—
ReactantBromineHCID 24408—
ReactantMethyl carbazateHCID 80519—
ReactantSodium FormateHCID 2723810—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventMethanol--water (1/1)HCID 22242641—
Productalpha-HydroxyacetophenoneHCID 68490—

Reaction Conditions

Temperature20 °C

Reaction Steps

A 100-gallon glass lined kettle equipped with a cooling jacket was charged with 90.5 lbs. of acetophenone, 123 lbs. of methanol and 340 mls. of 98% sulfuric acid. The reactor was cooled to 20° C and the mixture was stirred during the addition of 119 lbs. of bromine that was added incrementally by a gravity fed system at a rate so that the temperature was maintained at between 20°-25° C over a 3-hour period. After the bromination was complete, 37 lbs. of methanol, 240 lbs of water and 112 lbs. of sodium formate were added. The mixture was stirred with agitation overnight at 60° C and after cooling to 40° C a solution of 68 lbs. methyl carbazate in 45 lbs. of a 54:46 methanol-water mixture was added. The reaction mixture was stirred for 2-hours at 40° C to form the carbomethoxy nydrazone of α-hydroxy acetophenone. Thereafter the reaction mixture was allowed to cool to 20° C, was centrifuged, and washed with water on the centrifuge.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105848
Source datasetuspto-grants-1978_08
ORD IDord-3c777ec6682f484f8377f2cc7d343f6f
Source noteuspto-grants-1978_08