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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73971Generated: October 26, 2026

2-Bromoethanol → 2-(2-tert-Butyl-5-aminophenoxy)ethanol

https://huagongshe.com/reaction/73971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
Reactant2-Tert-butyl-5-nitrophenolHCID 21959617—
SolventAcetonitrileHCID 6342—
Product2-(2-tert-Butyl-5-aminophenoxy)ethanolHCID 57470212—

Reaction Steps

2-(2-tert-Butyl-5-aminophenoxy)ethanol (C-4) was synthesized following the general scheme above starting from 2-tert-butyl-5-nitrophenol (C-1-a) and 2-bromoethanol. HPLC ret. time 2.08 min, 10-99% CH3CN, 5 min run; ESI-MS 210.3 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-de1375ce261e4dac8fa5a72b344c4cf9
Source noteuspto-grants-2014_09