HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → S-(1,1-dimethylpropyl)ethylphosphonotrithioic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Amylthiol | HCID 15511 | — |
| Reactant | Phosphenodithioic ethane | HCID 16131073 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | S-(1,1-dimethylpropyl)ethylphosphonotrithioic acid | HCID 13715535 | — |
Reaction Steps
To a slurry of 16.5 grams (g) of ethylthionophosphine sulfide in tetrahydrofuran, under nitrogen at room temperature, was added 13.8 g (0.133 mole) 1,1-dimethyl-1-propanethiol (tertiary amyl mercaptan). To this mixture was added 18.5 milliliters (ml) (0.133 mole) triethylamine, dropwise. The mixture was stirred one hour at room temperature, then refluxed for 1/2 hour and stripped of solvent. There was obtained 30.1 g (87% of theoretical yield) of the triethylamine salt of S-(1,1-dimethylpropyl)ethylphosphonotrithioic acid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04614735 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-91f9ecc81e494faab7195e02189fbc62 |
| Source note | uspto-grants-1986_09 |