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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-2-(4-Nitrophenyl)oxirane | HCID 1237170 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Reactant | 2-(4-Iodo-phenoxy)-ethylamine | HCID 18543378 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (1R)-2-[[2-(4-iodophenoxy)ethyl]amino]-1-(4-nitrophenyl)ethanol | HCID 69103738 | 90.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417060B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-d3108714b2e9453badc21e45f82899b2 |
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| Source note | uspto-grants-2008_08 |
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