HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → 1-(3,4-Dihydro-2H-pyrano[2,3-b]pyridin-2-yl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 19791571 | HCID 19791571 | — |
| Product | 1-(3,4-Dihydro-2H-pyrano[2,3-b]pyridin-2-yl)methanamine | HCID 19791565 | 94.1% |
Reaction Steps
3.2 g (11 mmol) of the compound from Example VII and 9.2 g (150 mmol) of 2-aminoethanol are heated under nitrogen to 80° C. After 5 minutes the mixture is cooled, and the reaction mixture is partitioned between 70 ml of toluene and 92 ml of 5% strength NaCl solution. The phases are separated, and the aqueous phase is extracted with dichloromethane. The combined organic phases are dried and evaporated in vacuo. 1.7 g of the title compound are obtained as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250540 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-471e2a5674f843d88b89dfb159dcf82c |
| Source note | uspto-grants-1993_10 |