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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261075Generated: November 2, 2026

Acetic Acid → o-(Methylamino)phenol

https://huagongshe.com/reaction/2261075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzoxazoleHCID 9228—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Producto-(Methylamino)phenolHCID 69138—

Reaction Conditions

Temperature0 °C

Reaction Steps

1 g of benzoxazole was dissolved in 20 ml of THF. 0.9 g of NaBH4 were added under nitrogen and stirring. The suspension was cooled to 0° C. and 0.86 ml of acetic acid dissolved in 5 ml THF were slowly added, keeping the reaction temperature below 5° C. The reaction was stirred at 0° C. for 30 minutes and for further 12 hours at room temperature. The reaction mixture was again cooled to 0° C. and 50 ml of sat. NH4Cl solution were added carefully. The phases were separated and the aqueous layer extracted twice with EtOAc. The combined organic layers were washed with brine, dried over MgSO4 and filtered. Removal of the solvent afforded 0.97 g (of pure 2-(N-methylamino)-phenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846925B2
Source datasetuspto-grants-2010_12
ORD IDord-eacbc67941af4de19ad9810b0d0cedc4
Source noteuspto-grants-2010_12