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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618804Generated: October 31, 2026

Methanol → HCID 67258841, compound

https://huagongshe.com/reaction/1618804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzenamine, 2-phenoxy-HCID 75899—
Reactant1,3-Benzodioxole-4-carboxaldehydeHCID 82264—
ReactantSodium borohydrideHCID 4311764—
SolventFormic AcidHCID 284—
ProductHCID 67258841HCID 6725884151%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-phenoxy-phenylamine (410 mg, 2.22 mmol) and 2,3-(methylenedioxy)-benzaldehyde (500 mg, 3.33 mmol) was heated at 90° C. for 2 h under nitrogen. The reaction was cooled to 0° C. and MeOH (4 mL) was added, followed by NaBH4 (253 mg, 6.70 mmol) in portions over 20 min. The mixture was stirred at room temperature for 24 h. Formic acid (0.4 mL was added and the mixture stirred for 15 min. The solvents were removed in vacuo, the residue quenched with saturated aqueous NaHCO3 (50 mL), extracted with DCM (2×30 mL), dried over MgSO4, filtered and solvents removed in vacuo. The crude material was purified by silica gel chromatography eluting with petroleum spirit (A) and ethyl acetate (B) (5% B, 80 g, 4.0 CV, 60 mL/min) to afford 360 mg (51%) of N-(benzo[1,3]dioxol-4-ylmethyl)-N-(2-phenyloxy-phenyl) amine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08771641B2
Source datasetuspto-grants-2014_07
ORD IDord-cde44983d09e4c5e80ea5e144d252b74
Source noteuspto-grants-2014_07