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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096243Generated: October 29, 2026

Hydrochloric Acid → 4-Hydroxy-4-(thiazol-5-yl)cyclohexanone

https://huagongshe.com/reaction/2096243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant8-Hydroxy-8-(5-thiazolyl)-1,4-dioxaspiro[4.5]decaneHCID 59017441—
SolventDimethylformamideHCID 6228—
Product4-Hydroxy-4-(thiazol-5-yl)cyclohexanoneHCID 59017439—

Reaction Conditions

Temperature60 °C

Reaction Steps

A 5-L 4-neck round bottom flask equipped with a thermocouple, a mechanical stirrer, a condenser, and a nitrogen inlet/outlet adapter was charged with ketal 9 as prepared in the previous step (316.3 g, 1.30 mol) and DMF (238.0 mL) with stirring. A solution of 2 N HCl (1.13 L, 2.26 mol) was added over 2 min; the mixture was stirred at 26° C. for 5 min, warmed up to 60° C., and stirred for 3 h. The progress of the reaction was monitored by HPLC and LC-MS. The reaction was cooled to 0° C. in an ice-water bath, and the aqueous (pH=2˜3) was adjusted to an alkaline (pH=10˜11) by dropwise addition of 4 N NaOH solution with fast agitation. The resulting alkaline slurry was stirred at 0° C. for 1 h; the solid was collected by filtration, washed with cold water (100 mL), dried under air-suction for 1 h, and then placed in a vacuum drying oven under house vacuum (120 mmHg) at 50° C. for 48 h to afford the title compound, 10 as a beige crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450304B2
Source datasetuspto-grants-2013_05
ORD IDord-5d8a3c1cb4964240b2f74ec6803941b0
Source noteuspto-grants-2013_05