HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249232Generated: October 30, 2026
Water → Benzyl 3-formyl-1H-indole-1-carboxylate
https://huagongshe.com/reaction/1249232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Indole-3-Carboxaldehyde | HCID 10256 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 3-formyl-1H-indole-1-carboxylate | HCID 13711097 | 88% |
Reaction Steps
Sodium hydride (1.99 g, 50% in oil, 41.4 mmol, extracted with hexanes) was stirred in THF (50 ml) in a flame-dried flask at 0° C. under nitrogen. Indole-3-carboxaldehyde (5.00 g, 34.5 mmol) was added as a powder in small portions, and then the mixture was warmed to 40° C. for 30 min. The mixture was again cooled to 0° C., and benzyl chloroformate (4.92 ml, 34.5 mmol) was added. After warming to room temperature and stirring overnight, the mixture was poured into water (50 ml) and extracted with CH2Cl2 (50 ml). The organic layer was washed with water (50 ml), dried with MgSO4, filtered and evaporated to 9.2 g (95%) of a gold-brown oil. Crystallization from hot hexane gave 8.47 g (88%) of white crystalline product: mp 70°-71°
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04629794 |
|---|
| Source dataset | uspto-grants-1986_12 |
|---|
| ORD ID | ord-c5f5c7f62e084d32b44e8b1dc6485aaf |
|---|
| Source note | uspto-grants-1986_12 |
|---|