HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388271Generated: October 30, 2026
Hydrochloric Acid → HCID 178499332, compound
https://huagongshe.com/reaction/2388271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 178499327 | HCID 178499327 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178499332 | HCID 178499332 | — |
Reaction Steps
5-(3,3-Dimethyl-but-1-ynyl)-3-[(1,4-dioxa-spiro[4.5]dec-8-yl)-(trans-4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester (1 eq.) is dissolved in tetrahydrofuran and treated with 3.6 N HCl solution. The reaction is stirred at 40° C. for 5 h. Water is then added and the reaction mixture is cooled to room temperature. The reaction mixture is extracted with ethyl acetate (2×50 mL). The combined extracts are washed with 25 mL of aqueous saturated NaHCO3 and 2×50 mL of water. The organic layer is concentrated to a thick oil and 50 mL of heptane is added to the mixture to precipitate the desired compound which is filtered to give of 5-(3,3-dimethyl-but-1-ynyl)-3-[(trans-4-methyl-cyclohexanecarbonyl)-(4-oxo-cyclohexyl)-amino]-thiophene-2-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08269014B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-ebbc79d1cf09492e8dd15c6c40bc6741 |
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| Source note | uspto-grants-2012_09 |
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