HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017587Generated: October 30, 2026
Water → 2-(1-Methyl-1H-indol-3-YL)-2-oxoacetic acid methyl ester
https://huagongshe.com/reaction/1017587
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Methylindole | HCID 11781 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(1-Methyl-1H-indol-3-YL)-2-oxoacetic acid methyl ester | HCID 4453675 | 82.8% |
Reaction Steps
To a 0° C. solution of 1-methylindole (7.58 g, 50 mmoles) in dry ether (75 mL) under argon was added oxalyl chloride (4.36 mL, 50 mmoles) slowly. The resulting suspension was stirred for 30 minutes. After cooling to −65° C, sodium methoxide (22.9 mL, 100 mmoles, 25% in MeOH) was added dropwise at a rate to maintain −60° C. After the addition was complete, the reaction was allowed to warm to room temperature and stir for 2 hours. Water was added (30 mL) and the crude mixture was stirred then filtered. The resultant solid was washed with water, ether and then air dried. Purification of the crude product via flash chromatography (SiO2, 20% to 40% ethyl acetate/Hexane—gradient) provided methyl (1-methyl-1H-indol-3-yl)(oxo)acetate as a solid (9 g, 41.4 mmoles).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06479490B2 |
|---|
| Source dataset | uspto-grants-2002_11 |
|---|
| ORD ID | ord-c499bff7f78f4fd4880487ae88a57099 |
|---|
| Source note | uspto-grants-2002_11 |
|---|