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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129434Generated: October 26, 2026

2-Methyl-2-butanol → HCID 178463135, compound

https://huagongshe.com/reaction/129434

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-butanolHCID 6405—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPotassium CarbonateHCID 11430—
Reactant8-Fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxideHCID 15278521—
ReactantHCID 178418331HCID 178418331—
ProductHCID 178463135HCID 17846313576.8%

Reaction Steps

In a 50-ml flask, 0.70 g (0.0023 mol) of 8-fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxide, 0.28 g (0.0025 mol) of 1-ethyl-5-hydroxypyrazole and 0.52 g (0. 0025 mol) of DCC (N,N'-dicyclohexylcarbodiimide) were added to 5 ml of tert-amyl alcohol at the same time, and the mixture was stirred at room temperature for 30 minutes. Then, 0.17 g (0.00125 mol) of anhydrous potassium carbonate was added. The reaction mixture was allowed to react at 80° C. for 8 hours, and then the reaction solvent was distilled off under reduced pressure. The remainder was dispersed in a 2% potassium carbonate aqueous solution and ethyl acetate to separate it into two phases. Further, the aqueous phase was acidified with 5% hydrochloric acid, and the precipitated oil was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to give 0.70 g of 8-fluoro-4-methoxy-2,5-dimethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound 40) shown in Table 5. The yield thereof was 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468722
Source datasetuspto-grants-1995_11
ORD IDord-4fcb4cdc1c714c79bbfc206f222e3c19
Source noteuspto-grants-1995_11