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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14218Generated: October 25, 2026

Ethanolamine → Methyl 4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate

https://huagongshe.com/reaction/14218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantMethyl 4-butyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 21086200—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylateHCID 2108619880.1%

Reaction Steps

A solution of methyl 4-butyl-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate (800 mg) and 9-BBN (1.6 g) in tetrahydrofuran (13 mL) was refluxed for 1.5 h. The mixture was cooled to room temperature, ethanolamine (0.4 mL) was added, and the resulting solution was concentrated under reduced pressure. The residue was washed with hexanes, filtered, and the filtrate was concentrated under reduced pressure. Purification by flash column chromatography (silica, 25% ethyl acetate/hexanes) afforded 607 mg of the title compound: 1H NMR (300 MHz, DMSO-d6) δ 7.21, 7.16, 6.75, 4.24-4.21, 3.78, 3.34-3.24, 1.55-1.47, 1.38-1.30, 0.95-0.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-080904ae1a3f43bd8361146e18e6f260
Source noteuspto-grants-2010_06