HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167986Generated: October 25, 2026
Hexamethylphosphoramide → Ethyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylate
https://huagongshe.com/reaction/2167986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 3-Methyl-2-cyclohexen-1-one | HCID 14511 | — |
| Reactant | Ethyl cyanoformate | HCID 69336 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 2-hydroxy-6,6-dimethylcyclohex-1-enecarboxylate | HCID 67126375 | — |
Reaction Steps
Into a 500 mL flame dried round-bottomed flask was added copper(I) iodide (18 g) in ether (200 mL) to give a suspension. After cooling to −5° C., methyllithium (120 mL, 1.6M in ether) was added dropwise. After stirring at −5° C. for 1 hour, 3-methylcyclohex-2-enone (5.15 mL) in 15 ml ether was added dropwise, and the mixture was stirred at −5° C. for 1 hour. After cooling to −78° C., hexamethylphosphoramide (60 mL) was added dropwise. Ethyl carbonocyanidate (23.74 mL) was added. After stirring at −78° C. for 20 minutes, the mixture was warmed up to room temperature, and stirred for 1 hour. The mixture was poured into cold water, and the layers were separated. The aqueous layer was extracted with ether (3×20 mL). The combined organic layers were washed with saturated aqueous NH4Cl (3×20 mL), dried over Na2SO4, filtered, and dried under vacuum. The crude product was added to a silica gel column and purified by eluting with 0-10% ethyl acetate in hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045475B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-288b8a0eb3ae4f528672736f8193f8b6 |
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| Source note | uspto-grants-2015_06 |
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