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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859540Generated: October 26, 2026

Potassium Hydroxide → O-(2-Tert-butyl-4-formyl-5-methylphenyl) dimethylthiocarbamate

https://huagongshe.com/reaction/1859540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
Reactant5-tert-Butyl-4-hydroxy-2-methylbenzaldehydeHCID 11286988—
Reactantdimethylthiocarbamoyl chloride THFHCID 86592607—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductO-(2-Tert-butyl-4-formyl-5-methylphenyl) dimethylthiocarbamateHCID 9860485—

Reaction Conditions

Temperature45 °C

Reaction Steps

Ten percent KOH (80 mL) was added to a mixture of 5-tert-butyl-4-hydroxy-2-methylbenzaldehyde (Example T 99.0 g, 515 mmol) in water (180 mL) and THF (135 mL.) The mixture was treated with a solution of N,N-dimethylthiocarbamoyl chloride (86.1 g) in THF (108 mL) over a 2-hour period with simultaneous addition of 10% KOH in order to hold the pH of the reaction mixture between 12.0 and 12.3. After approximately 70% of the dimethylthiocarbamoyl chloride-THF solution had been added, vacuum was applied to the reaction mixture to remove the THF; during this distillation, the simultaneous additions of 10% KOH and the dimethylthiocarbamoyl chloride-THF solution were continued while maintaining the pH range between 12.0 and 11.6 and the reaction temperature between 23° C. to 25° C. The distillation was continued for 10 minutes after all the dimethylthiocarbamoyl chloride solution had been added. Stirring at ambient pressure and temperature was continued for another 90 minutes, during which time the pH was stable between 11.6 and 1.75. A solution of EtOAc (150 mL) and heptane (150 mL) was added to the reaction mixture, and after stirring and settling, the layers were separated and the aqueous layer extracted with 1:1 heptane:EtOAc. The combined organic extracts were extracted with 10% KOH (2×100 mL) and water (2×90 mL) and concentrated. The residue was diluted with MeOH (120 mL). The solution was warmed to 45° C. and H2O (20 mL) was added. The solution was cooled to room temperature. 50% NaOH (170 mg) was added, and the solution was concentrated. This residue was redissolved in MeOH (120 mL) at 50° C. and H2O (15 mL) was added. The solution was cooled slowly to −5° C. with the addition of dimethylthiocarbamic acid O-(2-tert-butyl-4-formyl-5-methyl-phenyl)ester seed crystals to promote crystallization. The mixture was filtered and the solid washed with 4:1 MeOH:H2O to give the title compound, mp 80-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528510B1
Source datasetuspto-grants-2003_03
ORD IDord-88c7cb9247c441f8b92a180c4ccaed2c
Source noteuspto-grants-2003_03