HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268510Generated: November 1, 2026
Sodium hydride → 1-[2-(1,2,3,4-Tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethyl]-1H-benzotriazole
https://huagongshe.com/reaction/2268510
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7-(2-Iodoethyl)-1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cycloheptene | HCID 18348518 | — |
| Reactant | HCID 178418385 | HCID 178418385 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[2-(1,2,3,4-Tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethyl]-1H-benzotriazole | HCID 18348597 | 78.3% |
Reaction Steps
To a suspension of sodium hydride (60% oil dispersion, 230 mg) in THF (6 ml) was added a solution of 1,2,3-benzotriazole (680 mg) in THF(6 ml) with cooling with ice. The reaction mixture was warmed to room temperature and stirred at ambient temperature for 30 min. 7-(2-Iodoethyl)-1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cycloheptene (1.20 g) was added and the stirring was continued for 12 hr. The reaction mixture was heated under reflux for 6 hr, diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride and dried. The solvent was removed in vacuo. The residue was purified by alumina column chromatography(hexane to hexane:ethyl acetate=4:1) and then with recrystallization from hexane-ethyl acetate to obtain the entitled compound (920 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06326369B1 |
|---|
| Source dataset | uspto-grants-2001_12 |
|---|
| ORD ID | ord-0cc3d7e49f8d4bd69bd6d49409d58320 |
|---|
| Source note | uspto-grants-2001_12 |
|---|