HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 8-[(2,2-Diethoxyethyl)sulfanyl]-10-oxodec-8-enenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2-diethoxy-ethanethiol | HCID 10942622 | — |
| Reactant | 10-Oxodec-8-enenitrile | HCID 54377058 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 8-[(2,2-Diethoxyethyl)sulfanyl]-10-oxodec-8-enenitrile | HCID 53888625 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 1.8 g of 9-cyano-2-nonenal, 1.4 g of 2,2-diethoxy-ethane-thiol and 50 μl of triethylamine is allowed to stand at room temperature for 48 hours. It is taken up in 100 ml of diethyl ether, the solution washed with water, dried and evaporated, to yield the 9-cyano-3-(2,2-diethoxy-ethylmercapto)-nonenal, showing in NMR spectrum peaks at 9.78, 4.55, 3.57 and 2.61 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04041047 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-c71cafe8a332404e91b282125dc4ca00 |
| Source note | uspto-grants-1977_08 |