HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485093Generated: October 31, 2026
(1-Methylcyclopropyl)methanol → HCID 118113349, compound
https://huagongshe.com/reaction/1485093
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (1-Methylcyclopropyl)methanol | HCID 137701 | — |
| Reactant | 6-Chloro-N-methoxy-N-methylnicotinamide | HCID 11435597 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118113349 | HCID 118113349 | 54% |
Reaction Steps
To a solution of potassium tert-butoxide (1.68 g) in tetrahydrofuran (30 mL), a solution of 1-methylcyclopropanemethanol (1.29 g) in tetrahydrofuran (5 mL) was added and the mixture was stirred at room temperature for 10 minutes. After the reaction mixture was cooled to 0° C., a solution in tetrahydrofuran (5 mL) of the compound (3.00 g) obtained in step (1) above was added and after being brought to room temperature, the reaction mixture was stirred for an hour. The reaction mixture was then concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=95:5-50:50) to give N-methoxy-N-methyl-6-[(1-methylcyclopropyl)methoxy]pyridine-3-carboxamide as a colorless oil (2.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09422240B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-f8eaa44371694385ae506730233af711 |
|---|
| Source note | uspto-grants-2016_08 |
|---|