HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21272043, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 54540393 | HCID 54540393 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21272043 | HCID 21272043 | 94% |
Reaction Steps
Oxalyl chloride (3.2 g, 2.2 mL, 24.7 mmol) was added dropwise under nitrogen to an ice cold solution of ethyl 7-(phenylmethoxy)-indole (2.3 g, 10.3 mmol) in anhydrous ether (40 mL). The mixture was stirred for 1 hour at room temperature during which time a yellow precipitate was formed. The solvent and the excess of oxalyl chloride was removed at reduced pressure to yield 7-(phenylmethoxy)-indol-3-yl-glyoxyl chloride. Ethanol (50 mL) was then added to the residue and the solution was stirred overnight under nitrogen at room temperature. Removal of the solvent in vacuo provided ethyl 7-(phenylmethoxy)-indol-3-yl-glyoxylate as a tan solid (3 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04810699 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-80bc4b64268849269feb2c47b02fcd26 |
| Source note | uspto-grants-1989_03 |