HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Mercaptoethanol → 2-[Methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | CID 71317501 | HCID 71317501 | — |
| Reactant | 2-[Dimethyl(2-sulfanylethoxy)silyl]oxyethanethiol | HCID 71602155 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[Methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol | HCID 86716163 | — |
Reaction Steps
The 2-[methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol (2) was synthesized according to the same procedure as 2-[dimethyl(2-sulfanylethoxy)silyl]oxyethanethiol (1), using triethylamine (8.08 g, 0.080 mol), trichloromethylsilane (3.98 g, 0.027 mol), and 2-mercaptoethanol (6.24 g, 0.080 mol) in ether (400 mL). 2-[methyl-bis(2-sulfanylethoxy) silyl]oxyethanethiol (2) was obtained as a clear, colorless, foul-smelling liquid (6.81 g, 93.2%). The product was purified by distillation under reduced pressure and obtained as a clear, colorless, foul-smelling liquid (4.53 g, 62.0%), Bp=128-129° C. at 0.25 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09243006B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-5341e6b9cf204074905f1e81a924ea78 |
| Source note | uspto-grants-2016_01 |