HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801345Generated: October 31, 2026
Cyclohexanecarboxylic acid → HCID 67441477, compound
https://huagongshe.com/reaction/1801345
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexanecarboxylic acid | HCID 7413 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67441230 | HCID 67441230 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67441477 | HCID 67441477 | 86% |
Reaction Steps
To an ice-cold mixture of 2-(4-fluoro-3-nitrophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate (0.3 mmol, 1.0 eq.), cyclohexanecarboxylic acid (0.46 mmol, 1.5 eq.), N,N-diisopropylethylamine (0.6 mmol, 2.0 eq.) in dichloromethane (5 mL) was added a solution of phosphorus oxychloride (0.36 mmol, 1.2 eq.). Then the reaction mixture was stirred at room temperature for 2.5 hours. LC-MS indicated that the starting material was consumed completely. The reaction was quenched by 20 mL water extracted with ethyl acetate (20 mL×2). The combined organic layer was concentrated and the residue was purified by column chromatography (petroleum ether/ethyl acetate=3:1) to afford methyl 2-(3-(cyclohexanecarboxamido)-4-fluorophenyl)-3,3-dimethyl-1,2,3,4-tetrahydroquinoline-6-carboxylate as a pale yellow solid; Yield: 86%; MS (ESI+APCI) M+1=439.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344137B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c6463fa790c24a92b1f95ebce033bf39 |
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| Source note | uspto-grants-2013_01 |
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