HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 68770660, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | HCID 14529092 | HCID 14529092 | — |
| Solvent | HOAc dioxane | HCID 22565020 | — |
| Product | HCID 68770660 | HCID 68770660 | 92% |
Reaction Steps
To a solution of acetic acid 1H-indol-6-yl ester (2.0 g, 11.4 mmol) in dioxane/acetic acid (1:1, 114 mL) was added formaldehyde (0.85 mL, 0.93 g, 11.4 mmol) and morpholine (1 mL, 1 g, 11.4 mmol) and the resulting mixture was stirred (rt, 16 h). The reaction mixture was concentrated in vacuo, diluted with DCM (200 mL) and washed with 1N NaOH (20 mL), 4 N NaOH (20 mL) and brine (2×10 mL). The organic layer was dried, filtered and concentrated in vacuo to provide the title compound (2.87 g, 92%). MS (ESI): mass calculated for C15H18N2O3, 274.1; m/z found, 275.1 [M+H]+. 1H NMR (600 MHz, CDCl3): 8.09 (s, 1H), 7.73 (d, J=8.5, 1H), 7.11 (dd, J=11.7, 2.1, 2H), 6.85 (dd, J=8.5, 2.0, 1H), 3.71-3.68 (m, 4H), 3.67 (s, 2H), 2.48 (s, 4H), 2.32 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399465B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-0e20ba4c313e44bab3785f3313b80078 |
| Source note | uspto-grants-2013_03 |