HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393315Generated: October 29, 2026
Chlorosulfonic acid → HCID 21883492, compound
https://huagongshe.com/reaction/393315
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | 2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylic acid | HCID 10131049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21883492 | HCID 21883492 | — |
Reaction Steps
To chlorosulfonic acid (50.0 mL) chilled to −15° C. was added 2-(trifluoromethyl)-2H-1-benzopyran-3-carboxylic acid (Example 10) (4.0 g, 16.7 mmol). After stirring at −15° C. for 1 hour, the solution was warmed to room temperature and stirred for 16 hours. The resulting solution was added dropwise over ice (100 mL) with two diethyl ether (2×75 mL) extractions. The diethyl ether layers were combined, washed with water (2×75 mL), and brine (2×75 mL, dried over sodium sulfate and concentrated in vacuo. The resulting solids were triturated with hexane-ethyl acetate (9:1, 100 mL). The 6-chlorosulfonyl-2-trifluoromethyl-2H-1-benzopyran-3-carboxylic acid was isolated as a white solid: mp 169-174. 1NMR (CD3OD/300 MHz) 8.18 (d, 1H, J=2.7 Hz), 8.06 (dd, 1H, J=8.7, 2.7 Hz), 7.93 (s, 1H), 7.28 (d, 1H, J=8.7 Hz), 6.00 (q, 1H, J=6.6 Hz). EIHRMS m/z 324.9977 (M+, Calcd 324.9994).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806288B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-6b062701c155452c84ff8b4b2f91ef0a |
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| Source note | uspto-grants-2004_10 |
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