HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalic Acid → HCID 21071558, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1H-Indole-3-ethanamine, 4-chloro- | HCID 6451401 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21071558 | HCID 21071558 | — |
Reaction Steps
Add dropwise oxalic acid (1.32 g, 1.3 eq.) in MeOH to a solution of 4-chlorotryptamine in EtOAc (2.2 g, 11.3 mmol) with vigorous stirring. When addition was complete, add Et2O to the cloud point and place flask in the freezer to give a solid. Collect the solid by filtration and wash with ether. Dry in a vacuum oven at room temperature to give the title compound as an off-white solid: 1H NMR (300 MHz, d6-DMSO): 3.11 (m, 2H), 3.2 (m, 2H), 7.04 (m, 2H), 7.34 (m, 2H), 11.44 (bs, 1H); MS (ES+): m/z 195 (M+H)+, 178 (M−NH2)+; (ES−): m/z 193 (M−H)−; Analysis for C12H13ClN2O4: Calcd.: C, 50.6263; H, 4.6026; N, 9.8396. found: C, 50.56; H, 4.57; N, 9.66.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044090B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-188ef535069240feb6e1b2de761c88b9 |
| Source note | uspto-grants-2011_10 |