HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082000Generated: October 25, 2026
2-Methyl-2-butanol → HCID 178463135, compound
https://huagongshe.com/reaction/1082000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 8-Fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxide | HCID 15278521 | — |
| Reactant | HCID 178418331 | HCID 178418331 | — |
| Product | HCID 178463135 | HCID 178463135 | 76.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05587484 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-d27bedaecb224c1384119b44b88346d0 |
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| Source note | uspto-grants-1996_12 |
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