HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromoethanol → 2-[(2-Pyridin-4-ylethyl)thio]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | 4-Pyridoethanethiol | HCID 150969 | — |
| Product | 2-[(2-Pyridin-4-ylethyl)thio]ethanol | HCID 2058406 | — |
Reaction Steps
Furthermore, by following this method 2-(4-pyridyl)ethyl mercaptan is reacted with 2-bromoethanol to yield 4-[2-(2-hydroxyethylthio)ethyl]pyridine, with 2-bromo-1-propanol to yield 4-[2-(2-hydroxy-1-propylthio)ethyl]pyridine, with 3-bromo-2-butanol to yield 4-[2-(3-hydroxy-2-butylthio)ethyl]pyridine, with ethyl 2-chloropropionate to yield ethyl 2-[2-(4-pyridyl)ethylthio]propionate, with methyl 2-phenyl-2-bromoacetate to yield methyl 2-phenyl-2-[2-(4-pyridyl)ethylthio]acetate, with alpha-bromoacetophenone to yield alpha-[2-(4-pyridyl)ethylthio]acetophenone, and with chloroacetone to yield 2-(4-pyridyl)ethylthioacetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04246263 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-b6a2ae8cc82d402bb4f73e482d4461b3 |
| Source note | uspto-grants-1981_01 |