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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416288Generated: November 1, 2026

1-Nitropropane → HCID 22638762, compound

https://huagongshe.com/reaction/2416288

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NitropropaneHCID 7903—
ReactantSodium HydroxideHCID 14798—
ReactantDiammonium hydrogen phosphateHCID 24540—
ReactantHCID 22638733HCID 22638733—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 22638762HCID 2263876238%

Reaction Steps

In 5 mL of acetic acid were combined the crude 6-(2-dimethylaminomethylcyclo-propyl)-1H-indole-3-carbaldehyde, ammonium hydrogen phosphate (0.99 g, 7.50 mmol), and nitropropane (0.09 g, 1.03 mmol.). The mixture was stirred and heated to a gentle reflux for 16 h. Water was added after cooling reaction to room temperature, and the mixture was made basic by the addition of 1 N NaOH. The mixture was extracted with methylene chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to give a brown oil. The oil was purified by flash chromatography (50% methanol/ethyl acetate) to give 6-(2-dimethylaminomethyl-cyclopropyl)-1H-indole-3-carbonitrile as an amber oil (93 mg, 38%). 1H NMR (CDCl3): δ 7.58 (m, 2H), 6.99 (m, 2H), 5.75 (s, 1H), 2.46 (m, 1H), 2.33 (s, 7H), 1.89 (m, 1H), 1.20 (m, 1H), 0.98 (m, 1H), 0.86 (m, 1H); FIMS: 238.2 (M−H); LCMS: 72% AP.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822100B2
Source datasetuspto-grants-2004_11
ORD IDord-ba809935b6fe4bb6a9ce3bc51eef847d
Source noteuspto-grants-2004_11