HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Methyl 8-cyano-2-[(2,2-diethoxyethyl)sulfanyl]octanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2,2-diethoxy-ethanethiol | HCID 10942622 | — |
| Reactant | Methyl 2-bromo-8-cyanooctanoate | HCID 20364819 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Methyl 8-cyano-2-[(2,2-diethoxyethyl)sulfanyl]octanoate | HCID 54422104 | — |
Reaction Steps
The starting material is prepared as follows: To the mixture of 13.6 g of methyl 2-bromo-8-cyano-octanoate, 11.6 g of 2,2-diethoxy-ethylmercaptan and 150 ml of methylene chloride, 5.56 g of triethylamine are added dropwise while stirring. After overnight-stirring at room temperature the mixture is evaporated, the residue triturated with diethyl ether, washed with water, dried and evaporated, to yield the methyl 2-(2,2-diethoxyethylmercapto)-8-cyano-octanoate showing NMR bands at 4.58, 3.71 and 2.75 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04041047 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-5a27c972a5574561a10ba91420a47abd |
| Source note | uspto-grants-1977_08 |