HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356223Generated: October 26, 2026
2-Bromoethanol → N-Ethyl-N-(beta-hydroxyethyl)-4-bromoaniline
https://huagongshe.com/reaction/356223
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-bromo-N-ethylaniline | HCID 11745656 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Ethyl-N-(beta-hydroxyethyl)-4-bromoaniline | HCID 18941473 | 69.5% |
Reaction Steps
17.3 g (86.7 mmols) of N-ethyl-4-bromoaniline, 22.7 ml (1.5-fold equivalent weight) of N,N-diisopropylethylamine and 9.64 ml (1.5-fold equivalent weight) of 2-bromoethanol were mixed, and the mixture obtained was heated at 125° C. for 2 hours in an atmosphere of argon. Next, to the reaction solution obtained, 1.5 ml (0.1-fold equivalent weight) of diisopropylethylamine and 0.64 ml (0.1-fold equivalent weight) of 2-bromoethanol were added, and the mixture obtained was heated at 125° C. for 3 hours in an atmosphere of argon. Water was added to the reaction solution obtained, which was then extracted with ethyl acetate. The organic layer obtained was dried with anhydrous magnesium sulfate and then concentrated. The residue thus obtained was purified by silica gel column chromatography developing system (chloroform) to obtain 14.7 g of N-ethyl-N-(2-hydroxyethyl)-4-bromoaniline (yield: 69.5%; a colorless oily liquid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05834575 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-007123975d5847128a691b561d3559d1 |
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| Source note | uspto-grants-1998_11 |
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