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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596714Generated: October 31, 2026

Acetovanillone → HCID 54457755, compound

https://huagongshe.com/reaction/1596714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetovanilloneHCID 2214—
ReactantPotassium HydroxideHCID 14797—
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 54457755HCID 54457755—

Reaction Steps

To a solution of acetovanillone (8.31 g, 50 mmol) and 2.81 g KOH (50 mmol) in H2O (34 mL), at 0°, is added a solution of dimethylthiocarbamoyl chloride (8.28 g, 67 mmol) in THF (14 mL), dropwise, at such a rate as to keep the reaction temperature below 12°. The reaction mixture is warmed to room temperature, and stirred for 30 minutes. It is then diluted with 1 N NaOH (100 mL) and extracted with EtOAc (3×80 mL). The combined organic phase is washed with H2O (1×100 mL) and brine (1×50 mL), dried over MgSO4, and concentrated in vacuo to give dimethylthiocarbamic acid O-(4-acetyl-2-methoxy-phenyl) ester. To a thick walled pyrex tube is aded dimethylthiocarbamic acid O-(4-acetyl-2-methoxy-phenyl) ester (9.81 g, 38.77 mmol). The tube is flushed with nitrogen, sealed, and then heated to 250° for 1 hour. After cooling, the residue is chromatographed (silica gel, 1:1 EtOAc/hexane) to yield dimethylthiocarbamic acid S-(4-acetyl-2-methoxy-phenyl) ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291530B1
Source datasetuspto-grants-2001_09
ORD IDord-82f2781546fe47abbc00106a115486e5
Source noteuspto-grants-2001_09