Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | But-3-yn-1-yl methanesulfonate | HCID 11378578 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(3-Butyn-1-yl)morpholine | HCID 10773054 | — |
Reaction Steps
A mixture of methanesulfonic acid but-3-ynyl ester (10.1 g, 68 mmol) and morpholine (12.5 mL, 143 mmol) was heated to 100° C. for 1 h. The mixture was diluted with Et2O (50 mL) and filtered. The solid residue was discarded, and the mother liquor extracted with 3N HCl. The aqueous layer was basified with NaOH, and back-extracted into EtOAc. Drying (Na2SO4), concentration, and distillation (short-path, b.p.=130° C. at ˜5 mm Hg) game the title compound as a colorless oil. 1H NMR (CDCl3) δ 3.72 (t, 4H), 2.60 (t, 2H), 2.48 (t, 4H), 2.39 (td, 2H), 2.00 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08093229B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-967a14a2464f4a9599f94f0c6669c5e3 |
|---|
| Source note | uspto-grants-2012_01 |
|---|