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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220392Generated: October 27, 2026

(R)-2-(4-Nitrophenyl)oxirane → (1R)-2-[[2-(4-iodophenoxy)ethyl]amino]-1-(4-nitrophenyl)ethanol

https://huagongshe.com/reaction/2220392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-(4-Nitrophenyl)oxiraneHCID 1237170—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
Reactant2-(4-Iodo-phenoxy)-ethylamineHCID 18543378—
SolventDimethyl SulfoxideHCID 679—
Product(1R)-2-[[2-(4-iodophenoxy)ethyl]amino]-1-(4-nitrophenyl)ethanolHCID 6910373890.3%

Reaction Steps

To a solution of [2-(4-iodophenoxy)ethyl]amine (6.14 g) in dimethyl sulfoxide (50 ml) was added N,O-bis(trimethylsilyl)acetamide (2.88 ml) and the mixture was stirred for 1 hour. To the mixture was added a solution of (2R)-2-(4-nitrophenyl)oxirane (3.21 g) in dimethyl sulfoxide (10 ml) and the mixture was stirred for 37 hours. After cooling to room temperature, the mixture was quenched by the addition of 5% acetic acid/water (120 ml) and stirred for 30 minutes. The mixture was basified with 1N sodium hydroxide and extracted with ethyl acetate (120 ml). The extract was washed with water (120 ml×2) and brine (120 ml), and dried over magnesium sulfate. Filtration followed by evaporation gave (1R)-2-[[2-(4-iodophenoxy)ethyl]amino]-1-(4-nitrophenyl)ethanol (7.52 g) as a brown solid. The compound was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417060B2
Source datasetuspto-grants-2008_08
ORD IDord-d3108714b2e9453badc21e45f82899b2
Source noteuspto-grants-2008_08