HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753766Generated: October 28, 2026
1,3-Dibromopropane → 4-(3-Bromopropoxy)-1-methyl-2-nitrobenzene
https://huagongshe.com/reaction/1753766
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Nitro-p-cresol | HCID 16271 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Bromopropoxy)-1-methyl-2-nitrobenzene | HCID 58962525 | — |
Reaction Steps
A solution of 4-methyl-3-nitrophenol (1.00 g, 6.53 mmol) in DMF (6 mL) was treated with K2CO3 (0.903 g, 6.53 mmol) and 1,3-dibromopropane (6.63 mL, 65.3 mmol) and heated to 100° C. for 2.5 h. The cooled mixture was diluted with water and extracted with DCM. The combined organics were dried (MgSO4), filtered and evaporated before purification by column chromatography (SiO2; eluting with 20% EtOAc in cyclohexane) to afford the desired product V-h as a mobile yellow oil (1.05 g, 59%). 1H NMR (300 MHz, CDCl3) δ 7.52 (d, J=2.7 Hz, 1H), 7.23 (d, J=8.5 Hz, 1H), 7.06 (dd, J=8.5, 2.7 Hz, 1H), 4.14 (t, J=5.8 Hz, 2H), 3.60 (t, J=6.4 Hz, 2H), 2.53 (s, 3H), 2.40-2.24 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09168245B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-e65c2599c21b4b5eab3704693ab7dcb3 |
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| Source note | uspto-grants-2015_10 |
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