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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439846Generated: October 30, 2026

Sodium Hydroxide → HCID 57223134, compound

https://huagongshe.com/reaction/439846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 14032101HCID 14032101—
SolventAcetic AcidHCID 176—
ProductHCID 57223134HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516788
Source datasetuspto-grants-1996_05
ORD IDord-7184d12b2b2148c2b21a7f2f102afecf
Source noteuspto-grants-1996_05