HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440128Generated: October 29, 2026
1,1-Dibromoethane → 1-Bromo-2-(4-benzyloxy-2-nitrophenoxy)ethane
https://huagongshe.com/reaction/440128
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyl-2-nitrophenol | HCID 786374 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-2-(4-benzyloxy-2-nitrophenoxy)ethane | HCID 22409159 | 139.3% |
Reaction Steps
A mixture of 4-benzyl-2-nitrophenol (1.3 g, 5.3 mmol) and K2CO3 (1.2 g, 8.7 mmol) in DMF (10 mL) was stirred for 10 min. Dibromoethane (1.4 mL, 16.2 mmol) was added to the reaction mixture and heated at 70° C. for 24 hrs. The reaction mixture was diluted with ether (30 mL) and washed with water (20 mL) and brine (20 mL). The ether layer was dried (MgSO4) and concentrated under reduced pressure. The crude product was fractionated by flash chromatography (4:1 hexane/ethyl acetate) yielding bromoethane 6 as a yellow oil (1.3 g, 88%). 1H NMR: 3.65 (t, J=5 Hz, 2H), 4.35 (t, J=5 Hz, 2H), 5.05 (s, 2H), 7.0-7.5 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05516911 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-d7573c1ee44e49548009e79c59c6e572 |
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| Source note | uspto-grants-1996_05 |
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