HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,6-Dibromohexane → 2-[2-[(6-Bromohexyl)oxy]ethyl]-6-methylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Reactant | 6-Methylpyridine-2-ethanol | HCID 70283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[2-[(6-Bromohexyl)oxy]ethyl]-6-methylpyridine | HCID 23045049 | 82.2% |
Reaction Steps
From 6-methyl-2-pyridineethanol (5 g) and 1,6-dibromohexane (26 g), stirring the reaction mixture under nitrogen for 18 h, and using ethyl acetate for extraction. FCC eluting with cyclohexane→cyclohexane-ethyl acetate (92:8) gave the title compound as a yellow oil (9 g), t.l.c. (System A 80:20:1) Rf 0.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937251 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-bfe72a7401c145ce9e3457386b7853d9 |
| Source note | uspto-grants-1990_06 |