HuagongsheHuagongshe Chemistry Print Report · For research reference only
Octanoyl chloride → S-{3-[(Dimethoxymethyl)silyl]propyl} octanethioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Octanoyl chloride | HCID 8124 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 169231 | HCID 169231 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | S-{3-[(Dimethoxymethyl)silyl]propyl} octanethioate | HCID 71417114 | 96% |
Reaction Steps
Octanoyl chloride (18.0 g, 0.111 mol) is added dropwise over 30 minutes to a solution of 3-mercaptopropyldimethoxymethylsilane F with CAS number [31001-77-1] (20.0 g, 0.111 mol) and triethylamine (11.2 g, 0.111 mol) in cyclohexane (200 mL) kept at 5° C. under an inert atmosphere. The temperature of the reaction medium remains between 5 and 8° C. The reaction medium is then stirred for 15 hours at room temperature. The precipitate of triethylamine hydrochloride Et3N.HCl is filtered over celite. After evaporating the solvents under reduced pressure at 25° C., S-octanoylmercaptopropyl-dimethoxymethylsilane G with CAS number [828241-23-2] (32.6 g, 0.106 mol) is obtained in the form of a colourless oil with a yield of 96%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08623937B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-0afc97b9864346b7b160a8aa8e941d4e |
| Source note | uspto-grants-2014_01 |