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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601561Generated: October 29, 2026

Acetate → 4-Benzyl-2,2-dimethylmorpholine

https://huagongshe.com/reaction/601561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[Benzyl(2-methylprop-2-EN-1-YL)amino]ethan-1-OLHCID 57421500—
CatalystMercuryHCID 23931—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-2,2-dimethylmorpholineHCID 1557911154%

Reaction Steps

Add 2-[benzyl-(2-methyl-allyl)-amino]-ethanol (13.0 g, 63.2 mmol) to a slurry of mercury (It) acetate (20.7 g, 65.0 mmol) in water (45 mL) and THF (45 mL). After 3 h, treat the mixture with NaOH (25 mL, 2.5 M aqueous, 125 mmol) followed by NaBH4 (2.72 g, 71.9 mmol). After 19 h, decant the mixture away from the metallic mercury and add to a separatory funnel with tert-butyl methyl ether (250 mL). Separate the organic solution, wash with water (250 mL), filter through a silica plug, and concentrate. Purify the residue by flash chromatography using a gradient from 5% to 10% tert-butyl methyl ether in CH2Cl2. Collect and concentrate the fractions containing product then dissolve the residue in hexanes (100 mL). Filter the solution through Celite® to remove metallic mercury and then concentrate the filtrate to give the title compound (7.01 g, 54%) as a colorless liquid. 1H NMR (DMSO-d6, 400 MHz) δ 7.20-7.40 (5H, m), 3.60 (2H, m), 3.42 (2H, s), 2.29 (2H, m), 2.10 (2H, s), 1.14 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902356B2
Source datasetuspto-grants-2011_03
ORD IDord-37c08aa48852434494165117eb9d1adc
Source noteuspto-grants-2011_03