HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → ETHYL (1-CYANOCYCLOHEXYL)ACETATE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 21652232 | HCID 21652232 | — |
| Product | ETHYL (1-CYANOCYCLOHEXYL)ACETATE | HCID 10965422 | 74% |
Reaction Steps
26.9 g (100 mmol) of (1-cyanocyclohexyl)malonic acid dimethyl ester, 4.3 g (100 mmol) or lithium chloride and 3.6 g (200 mmol) of water were heated in 300 ml of dimethyl sulfoxide for 22 hours to 150° C. Then it was cooled, mixed with 700 ml of water and extracted with 1000 ml of pentane. 14.4 g of (1-cyanocyclohexyl)acetic acid ethyl ester was obtained by distillation of the organic phase, corresponding to a yield of 74 percent (relative to the (1-cyanocyclohexyl)malonic acid dimethyl ester used). Data for the product was:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05136091 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-d375a53009ed485c8f87ab38ddf99739 |
| Source note | uspto-grants-1992_08 |