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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068Generated: October 26, 2026

Dicyclohexylcarbodiimide → HCID 178418286, compound

https://huagongshe.com/reaction/1068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4,5,8-Tetramethylthiochroman-6-carboxylic acid-1,1-dioxideHCID 15869804—
ReactantThiochroman carboxylic acidHCID 19693770—
ReactantHCID 178418331HCID 178418331—
ReactantHCID 178418394HCID 178418394—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 178418286HCID 17841828662.6%

Reaction Steps

7.4 Grams (0.026 mol) of 4,4,5,8-tetramethylthiochroman-6-carboxylic acid-1,1-dioxide corresponding to thiochroman carboxylic acid (IIIc), 3.4 g (0.03 mol) of 1-ethyl-5-hydroxypyrazole corresponding to 5-hydroxypyrazole (II) and 6.22 g (0.03 mol) of DCC (N,N'-dicyclohexylcarbodiimide) were all together added to 50 ml of tert-amyl alcohol, and the mixture was stirred at room temperature for 30 minutes. Then, 1.8 g (0.013 mol) of anhydrous potassium carbonate was added. The reaction mixture was allowed to react at 80° C. for 8 hours, and the reaction solvent was distilled off under reduced pressure. The resultant residue was dispersed in a 5% potassium carbonate aqueous solution and ethyl acetate to separate it into two layers. Further, the aqueous layer was adjusted to a pH of 1 with 5% hydrochloric acid, and the formed solid was recovered by filtration to give 6.13 g (yield 62%) of 4,4,5,8-tetramethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound Ic-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723408
Source datasetuspto-grants-1998_03
ORD IDord-c66dc862259d4aac940736920bae0111
Source noteuspto-grants-1998_03