HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethane, 2-bromo-1,1-diethoxy- → 4-(2,2-Diethoxyethylthiomethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Pyridin-4-ylmethanethiol | HCID 13092602 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2,2-Diethoxyethylthiomethyl)pyridine | HCID 13092603 | — |
Reaction Steps
Under a nitrogen atmosphere, sodium methoxide (0.60 g., 11 moles) is dissolved in approximately 15 ml. of stirring ethanol and cooled in an ice bath. 4-Picolyl mercaptan (1.4 g., 11 mmoles) in approximately 3 ml. of absolute ethanol is added over 5 minutes and the mixture stirred for 15 minutes. Bromoacetaldehyde diethylacetal (2.4 g., 11 mmoles) in approximately 15 ml. of absolute ethanol is then added over 5 minutes. The reaction mixture is warmed to room temperature and stirred for 16 hours. The reaction mixture is filtered and the filtrate evaporated to yield title product, which if desired, can be further purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04371696 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-aa6bac146274468a911ce5a31e67e2e6 |
| Source note | uspto-grants-1983_02 |