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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576023Generated: November 1, 2026

Phenol → 2-Phenoxyethanamine

https://huagongshe.com/reaction/576023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantEthylenediamineHCID 3301—
ReactantPotassium HydroxideHCID 14797—
ReactantMAGNESIUM SILICATE (synthetic)HCID 61680—
Reactant2-OxazolidinoneHCID 73949—
Product2-PhenoxyethanamineHCID 1565184.3%

Reaction Steps

To a 250 mL round bottom flask equipped with a thermocouple, heating mantle, nitrogen inlet/outlet, a condenser and a stir bar was added 2-oxazolidinone (14.8 g, 170 mmole), phenol (10.0 g, 106.3 mmole), potassium hydroxide (596 mg, 10.6 mmole) and ExxonMobil™ Aromatic 100 solvent (100 mL). The resulting mixture was heated to reflux temperature for 3 h. Reaction progress was monitored by TLC and 1H NMR. Once the phenol was consumed, ethylenediamine (3.6 mL, 53 mmole) was added and the reaction mixture was continued to stir at reflux temperature for 2 hrs. The reaction mixture was then cooled to room temperature. Florisil® (5 g) was added and the reaction mixture was filtered over Celite. The reactor and the filter cake were washed with ExxonMobil™ Aromatic 100 solvent (2×10 mL). The combined filtrates were concentrated under reduced pressure to give 12.3 g (84%) of the desired product as a yellow oil. Purity level was determined by NMR to be ˜95%. 1H NMR (CDCl3, 400 MHz) δ 7.22-7.14 (m, 2H), 6.89-6.77 (m, 3H), 3.80 (dd, 2H, J=5.3, 5.3 Hz)), 2.90 (dd, 2H, J=5.4, 5.4 Hz), 1.41 (bs, 2H), 13C NMR (CDCl3, 400 MHz) 158.9, 129.4, 120.7, 114.4, 70.0, 41.5, MS (ESI) for C8H11NO [M+H] calc. 137.08. found 137.56.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035097B2
Source datasetuspto-grants-2015_05
ORD IDord-6f5e86b0d71c41a389b1c97690d437be
Source noteuspto-grants-2015_05