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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324650Generated: October 29, 2026

Water → 2-(1,2,3,7,8,9-Hexahydroindeno[5,4-b][1,4]oxazin-9-yl) ethylamine

https://huagongshe.com/reaction/324650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant9-(2-aminoethyl)-1,7,8,9-tetrahydro-indeno[5,4-b][1,4]oxazin-2(3H)-oneHCID 11128171—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(1,2,3,7,8,9-Hexahydroindeno[5,4-b][1,4]oxazin-9-yl) ethylamineHCID 11769937—

Reaction Steps

A solution of 9-(2-aminoethyl)-1,7,8,9-tetrahydroindeno[5,4-b][1,4]oxazin-2(3H)-one (1.2 g, 5.3 mmol.) in tetrahydrofuran (30 mL) was was cooled with ice, to which was added lithium aluminum hydride (0.8 g, 21.4 mmol.). The mixture was heated for 18 hours under reflux under argon atmosphere. The reaction mixture was cooled, to which were added water (0.8 mL), a 15% aqueous solution of sodium hydroxide (0.8 mL) and water (2.4 mL), successively. The mixture was then stirred for 30 minutes at room temperature. Insolubles were filtered off, and the filtrate was concentrated under reduced pressure. Then, in substantially the same manner as in Example 36, from 2-(1,2,3,7,8,9-hexahydroindeno[5,4-b][1,4]oxazin-9-yl) ethylamine thus obtained and propionic acid, the title compound was produced (yield 250 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218429B1
Source datasetuspto-grants-2001_04
ORD IDord-b32d065af6fc4e37bf880c74a8f9553f
Source noteuspto-grants-2001_04