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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788819Generated: October 27, 2026

N-[3-{(1,4-benzodioxan-2-ylmethyl)amino}propionyl]-3,4-methylenedioxyaniline → HCID 13210215, compound

https://huagongshe.com/reaction/1788819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[3-{(1,4-benzodioxan-2-ylmethyl)amino}propionyl]-3,4-methylenedioxyanilineHCID 13210223—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13210215HCID 1321021597.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

In 50 ml of tetrahydrofuran is suspended 1.5 g of lithium aluminum hydride and a solution of 6.0 g of N-[3-{(1,4-benzodioxan-2-yl}methyl)amino propionyl]-3,4-methylenedioxyaniline prepared according to the procedure described in Example 6 dissolved in 10 ml of tetrahydrofuran is added dropwise to the suspension. After completion of the dropwise addition, the mixture is stirred for 4 hours at 50° C. After completion of the reaction, the reaction mixture is subjected to the post-treatment for lithium aluminum hydride in the conventional manner and the resulting precipitates including aluminum hydroxide are removed by filtration. The filtrate is concentrated and then dissolved in ethyl acetate and the resulting solution is washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. Thereafter, 20% hydrogen chloride in ethyl acetate is added and the resulting crystals are collected by filtration and recrystallized from ethanol to give 5.6 g (80%) of N-[3-{(1,4-benzodioxan-2-ylmethyl)amino}propyl]-3,4-methylenedioxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684739
Source datasetuspto-grants-1987_08
ORD IDord-ee7884ce19df458082f8329aee02b602
Source noteuspto-grants-1987_08