HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439844Generated: October 30, 2026
Sodium Hydroxide → HCID 1229702, compound
https://huagongshe.com/reaction/439844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 19780370 | HCID 19780370 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 1229702 | HCID 1229702 | — |
Reaction Steps
5,10-Dihydro-8-iso-propylindeno [1,2-b]indole (5.27 g, 21.3 mmol) was stirred at room temperature in glacial acetic acid (100 cm3). Sodium cyanoborohydride (5 g, 3 equivalents) was added portionwise over a period of 30 minutes. The reaction was stirred for a further 30 minutes, and then poured into ice/water (150 cm3). After stirring for 30 minutes, the solution was neutralised with aqueous sodium hydroxide, and the colourless solid thus formed collected by filtration. This solid was washed copiously with water until the residue was free from cyanide ion and then dried in a vacuum oven to give the title compound as a colourless solid. Yield: 3.25 g (61%). M.p. 104° C. [from petrol (60°-80° C.)]. 1H NMR (CDCl3) δ: 1.19 (6H, d,), 2.80 (1H, septet,), 3.20 (1H, dd,), 3.48 (1H, dd,), 4.07 (1H, br,), 4.15 (1H, ddd,), 5.21 (1H, d,), 6.53 (1H, d,), 6.86 (1H, dd,), 7.03 (1H, s,), 7.1-7.4 (4H, m,).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05516788 |
|---|
| Source dataset | uspto-grants-1996_05 |
|---|
| ORD ID | ord-373ed67b0bf649f1902d39508f6af881 |
|---|
| Source note | uspto-grants-1996_05 |
|---|