Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 4-methylidenecyclohexane-1-carboxylate | HCID 15151435 | — |
| Reactant | HCID 86635726 | HCID 86635726 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57951459 | HCID 57951459 | — |
Reaction Steps
A solution of 1-chloro-1-hydroxyiminomethyl-3-methoxybenzene (31 g, 167 mmol) in DCM (50 ml) was slowly added dropwise to a solution of 4-methylenecyclohexanecarboxylic acid ethyl ester (28 g, 167 mmol) in DCM (950 ml) at 0° C. Subsequently, a solution of triethylamine (50 ml) in DCM (50 ml) was slowly added dropwise at 0° C. and the resulting mixture was stirred overnight at RT. The reaction mixture was diluted with water (500 ml). The combined organic phases were washed with 10% aq. citric acid solution (800 ml) and sat. aq. NaCl solution (500 ml), dried over sodium sulphate and the solvent was removed under vacuum. The desired product 3-(3-methoxyphenyl)-1-oxa-2-azaspiro[4.5]dec-2-ene-8-carboxylic acid ethyl ester (51 g) was reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981883B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-33e722d57ef94893827cb02f81e1bc13 |
|---|
| Source note | uspto-grants-2011_07 |
|---|