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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598068Generated: October 26, 2026

Hydrochloric Acid → 8-(2,4-Dimethylphenyl)-2-methyl-4-(1-propylbutyl)-3,4-dihydro-2H-1,4-benzoxazine

https://huagongshe.com/reaction/598068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant8-(2,4-Dimethylphenyl)-2-methyl-4-(1-propylbutyl)-2H-1,4-benzoxazin-3(4H)-oneHCID 58938601—
SolventTetrahydrofuranHCID 8028—
Product8-(2,4-Dimethylphenyl)-2-methyl-4-(1-propylbutyl)-3,4-dihydro-2H-1,4-benzoxazineHCID 5893861631%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 8-(2,4-dimethylphenyl)-2-methyl-4-(1-propylbutyl)-2H-1,4-benzoxazin-3(4H)-one (50 mg, 0.14 mmol) was added dropwise to borane-tetrahydrofuran complex (1M solution in tetrahydrofuran, 1.37 ml, 1.4 mmol) in tetrahydrofuran (2 ml) with ice-cooling. The mixture was refluxed for 24 h and then decomposed at room temperature by dropwise addition of 6N hydrochloric acid (2 ml). The mixture was stirred at 50° C. for 30 min. The acidic solution was made alkaline with excess ammonium hydroxide, and the basic mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and concentrated under vacuum. The residue was purified by column chromatography eluting with 1% ethyl acetate/n-hexane to afford 15 mg (31%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897607B2
Source datasetuspto-grants-2011_03
ORD IDord-daf28040c9764131ac3d9df0b3df6552
Source noteuspto-grants-2011_03