HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439846Generated: October 30, 2026
Sodium Hydroxide → HCID 57223134, compound
https://huagongshe.com/reaction/439846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 14032101 | HCID 14032101 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57223134 | HCID 57223134 | — |
Reaction Steps
5,10-Dihydro-2-methoxy-1,3-dimethylindeno[1,2-b]indole (1 g, 3.80 mmol) was stirred at room temperature in glacial acetic acid (15 cm3). Sodium cyanoborohydride (0.75 g, 3 equivalents) was added portionwise over 15 minutes, and the reaction stirred for a further two hours. The reaction was poured into ice/water (30 cm3), and stirred for a further 30 minutes. The solution was neutralised with aqueous sodium hydroxide, and extracted into diethyl ether. The organic extracts were copiously washed with water until the washings were free of cyanide ion. The solvent was removed in vacuo to give the title compound. This was purified by column chromatography to a colourless solid. Yield: 0.8 g (79%). M.p. 117° C. from EtOAc/petrol (60°-80° C.). Elementary analysis: Found: C 81.6, H 7.3, N 5.8, C18H19NO Calc. for C 81.5, H 7.2, N 5.9, 1H NMR (CDCl3) δ: 2.15 (3H, s,), 2.25 (3H, s,), 3.07 (1H, dd,), 3.36 (1H, dd,), 3.64 (3H, s,), 4.1 (1H, br,), 4.19 (1H, ddd,), 5.20 (1H, d,), 6.60 (1H, d,), 6.74 (1H, ddd,), 6.97 (1H, s,), 7.00 (1H, ddd,), 7.17 (1H, d,).
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-7184d12b2b2148c2b21a7f2f102afecf |
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| Source note | uspto-grants-1996_05 |
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