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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275472Generated: November 4, 2026

Dicyclohexylcarbodiimide → HCID 22118399, compound

https://huagongshe.com/reaction/1275472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHCID 22118368HCID 22118368—
ReactantHCID 178418331HCID 178418331—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 22118399HCID 2211839996.2%

Reaction Steps

1.5 Grams (4.9 mmol) of 3,4-dichloro-5-methyl-6-carboxythiochroman-1,1-dioxide was dissolved in 5 ml of t-amyl alcohol, and 1.1 g (5.3mmol, 1.2 eq.) of 1-ethyl-5-hydroxypyrazole and 1.1 g (5.3 mmol, 1.2 eq.) of N,N'-dicyclohexylcarbodiimide were added. The mixture was stirred at room temperature for 2.5 hours. After the completion of the reaction, the reaction mixture was extracted with ethyl acetate and hexane, and liberated N,N'-dicyclohexylurea was filtered off. An organic layer was concentrated under reduced pressure and purified by column chromatography (silica gel/ethyl acetate) to give 1.9 g (yield 95%) of 3,4-dichloro-5-methyl-6-(1-ethylpyrazol-5-yl)oxycarbonylthiochroman-1,1-dioxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159904
Source datasetuspto-grants-2000_12
ORD IDord-d49b2f10438a44b1b847841424854528
Source noteuspto-grants-2000_12