HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439843Generated: October 31, 2026
Sodium Hydroxide → HCID 57079581, compound
https://huagongshe.com/reaction/439843
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 8-Methyl-5,10-dihydroindeno[1,2-b]indole | HCID 22247079 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57079581 | HCID 57079581 | — |
Reaction Steps
5,10-Dihydro-8-methylindeno[1,2-b]indole (10 g, 46 mmol) was stirred at room temperature in glacial acetic acid (150 cm3). Sodium cyanoborohydride (8.6 g, 3 equivalents) was added portionwise over a period of 30 minutes. The reaction was stirred for a further hour, and then poured into ice/water (200 cm3). After stirring for 30 minutes, the acidic solution was made basic by the addition of 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 yield the title compound as a colourless solid. Yield: 7.5 g (73%) M.p. 110° C. (from ethanol/water). 1H NMR (CDCl3) δ: 2.24 (3H, s,), 3.20 (1H, dd,), 3.50 (1H, dd,) 3.9 (1H, br,), 4.16 (1H, dd,), 5.23 (1H, d,), 6.52 (1H,d,), 6.80 (1H, d,), 6.99 (1H, s,), 7.1-7.4 (4H, m,).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516788 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-ca0f4c6f72a8490da954a345f5cf53e7 |
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| Source note | uspto-grants-1996_05 |
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