HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985949Generated: October 30, 2026
5-Chlorothiophene-2-sulfonyl chloride → HCID 68429355, compound
https://huagongshe.com/reaction/1985949
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Chlorothiophene-2-sulfonyl chloride | HCID 2733925 | — |
| Reactant | HCID 45027014 | HCID 45027014 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 68429355 | HCID 68429355 | — |
Reaction Steps
The amino(4,4-difluorocyclohexyl)acetic acid (2.68 g, 10.973 mmol) was dissolved in 2N NaOH (20 mL). The solution was cooled to 0° C., 5-chlorothiophene-2-sulfonyl chloride (3.25 g, 12.42 mmol) was added (5 min) dropwise as a solution in THF (10 mL). The solution was allowed to warm up to 25° C. overnight. After 19 h, THF was removed in vacuo and the mixture was acidified to a pH of about 1 to about 2 with 2N HCl (20 mL). The aqueous layer washed with EtOAc (4×50 mL). The combined organic layers were dried over MgSO4, filtered, and concentrated to produce {[(5-chlorothien-2-yl)sulfonyl]amino}(4,4-difluorocyclohexyl)acetic acid as a crude oil (3.8 g, 98.2%). Mass Spectrum (−ESI): 372 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547725B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-725e502d8d6e4e8b9605a3033d8d5e6b |
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| Source note | uspto-grants-2009_06 |
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