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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670461Generated: October 30, 2026

Ethanolamine → HCID 57699419, compound

https://huagongshe.com/reaction/1670461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant(2R)-2-(3,4-dichlorophenyl)oxiraneHCID 10352473—
SolventIsopropanolHCID 3776—
ProductHCID 57699419HCID 57699419100%

Reaction Steps

In a 3 neck flask equipped with a mechanical stirrer, thermocouple and addition funnel in an ambient temperature water bath was added ethanolamine (330 mL, 5.47 mol). (R)-2-(3,4-dichlorophenyl)oxirane (184 g, 976 mmol) in isopropanol (75 mL) was added dropwise over 1 h. Reaction temperature stayed <30° C. during addition. The reaction mixture was stirred at ambient temperature for 14 h, diluted with 2000 mL of ice water and extracted three times with 1000 mL of ethyl acetate. The combined organic phases were dried over MgSO4, filtered over Celite and concentrated in vacuo affording (1R)-1-(3,4-dichlorophenyl)-2-(2-hydroxyethylamino)-ethanol (244 g, 100%) as a white semi-solid. 1H-NMR (400 MHz, CDCl3) δ 7.58-7.54 (m, 2H), 7.35-7.32 (m, 1H), 5.51 (s, 1H), 4.64 (dd, J=5.0, 7.2 Hz, 1H), 4.49 (s, 1H), 3.43 (dd, J=5.0, 10.4 Hz, 2H), 2.69-2.50 (m, 4H). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=250.3; tR=0.84 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994166B2
Source datasetuspto-grants-2011_08
ORD IDord-ec541de9cfe04d828ec2bea9941ffaa7
Source noteuspto-grants-2011_08