HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253164Generated: October 25, 2026
Potassium Carbonate → (2S)-2,3-dihydro-1-[(3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-yl)sulfonyl]indole-2-carboxylic acid
https://huagongshe.com/reaction/253164
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Indoline-2-carboxylic acid, (S)- | HCID 2733920 | — |
| Reactant | 2,2-Dimethyl-6-Chromanesulfonyl Chloride | HCID 2779774 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2S)-2,3-dihydro-1-[(3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-yl)sulfonyl]indole-2-carboxylic acid | HCID 66845811 | 73% |
Reaction Steps
1 g (6.13 mmol) of 2,3-dihydro-(2S)-1H-indole-2-carboxylic acid, and 0.97 g (7.05 mmol) of potassium carbonate are solubilised in 2 ml of water. 1.6 g (6.13 mmol) of 3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-sulfonyl chloride solubilised in 12 ml of acetonitrile and 2 ml of water are added. Agitation is allowed to take place for 5 hours at ambient temperature. Water is added to the reaction medium, washing is performed with ethyl acetate, the acidity of the aqueous phase is raised to pH 3 by a solution of hydrochloric acid 1 N, and then extraction is performed using ethyl acetate. The organic phases are collected, dried on magnesium sulfate, filtered and concentrated under reduced pressure. The evaporation residue is purified by silica column chromatography eluting with the help of a dichloromethane/methanol (9/1; v/v) mixture. The expected product is obtained in the form of a beige foam with a yield of 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872021B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-2219d297833a45b8bd1d6439377e0d1c |
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| Source note | uspto-grants-2011_01 |
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