HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 15082735, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 15082721 | HCID 15082721 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 15082735 | HCID 15082735 | — |
Reaction Steps
5,10-Dihydro-8-methoxyindeno[1,2-b]indole (770 mg, 3.3 mmol) was reacted with sodium cyanoborohydride (1.0 g, 16 mmol), in glacial acetic acid (17 cm3) solution. After 30 minutes, the solution was poured into ice/water, stirred for 1 hour, and neutralised with sodium hydroxide. The colourless reaction mixture was extracted into diethylether, the organic layers, dried (Na2SO4), and concentrated in vacuo. The residue was column chromatographed (10% ethyl acetate/petrol 60°-80° C.) to yield the title compound as a colourless solid. Yield: 520 mg (66%). M.p. 101° C. 1H NMR (CDCl3) δ: 3.28 (1H, dd,), 3.57 (1H, dd,), 3.80 (3H, s,), 3.85 (1H, br,), 4.24 (1H, dd,), 5.30 (1H, d,), 6.6-7.4 (7H, m,).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05516788 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-ae18a2b3bdf74641b9c9a258f303d4cd |
| Source note | uspto-grants-1996_05 |