HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412242Generated: October 29, 2026
Sodium Hydroxide → 3-(Methoxycarbonyl)cyclohexane-1-carboxylic acid
https://huagongshe.com/reaction/412242
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dimethyl cyclohexane-1,3-dicarboxylate | HCID 138896 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Methoxycarbonyl)cyclohexane-1-carboxylic acid | HCID 317553 | 57.1% |
Reaction Steps
To a solution of 1,3-cyclohexanedicarboxylic acid (10 g, 58 mmol) in MeOH (50 mL) was added conc. H2SO4 (2 mL). Then the mixture was stirred at room temperature for 4 hrs. The mixture was concentrated under reduced pressure, and then partitioned between ethyl acetate and a saturated aqueous NaHCO3 solution. The organic phase was washed with brine, dried over Na2SO4, and evaporated to give dimethyl 1,3-cyclohexanedicarboxylate as a colorless oil (11.6 g, yield; quant.). To a solution of dimethyl 1,3-cyclohexanedicarboxylate (11.6 g, 57.9 mmol) in MeOH (58 mL) was added a 1N NaOH solution (58 mL) dropwise over 1 hr at 0° C. The resulting mixture was stirred at 0° C. for 0.5 hrs, and at room temperature for 2 hrs. The mixture was concentrated under reduced pressure, and the residual solution was partitioned between ethyl acetate and water. The aqueous phase was separated, acidified with conc. HCl (15 mL), saturated with NaCl, and then extracted with ethyl acetate. The extract was dried over Na2SO4, filtered and concentrated under reduced pressure to give 3-(methoxycarbonyl)cyclohexanecarboxylic acid as a colorless oil (6.16 g, yield; 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562811B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-f660fbfd593147c8a16f1589980ad5d7 |
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| Source note | uspto-grants-2003_05 |
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