HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77293Generated: October 28, 2026
Ethanolamine → HCID 57699419, compound
https://huagongshe.com/reaction/77293
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | (2R)-2-(3,4-dichlorophenyl)oxirane | HCID 10352473 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 57699419 | HCID 57699419 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841282B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-6694b905d3e14b5f8b6ac339eb25d977 |
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| Source note | uspto-grants-2014_09 |
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