HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Benzyloxy-2-chloro-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chloro-3-nitrophenol | HCID 69127 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Benzyloxy-2-chloro-nitrobenzene | HCID 11043622 | 93.4% |
Reaction Steps
This was prepared as follows:- A solution of benzyl bromide (10.26 g; 60 mmol) and 4chloro-3-nitrophenol (8.7 g; 50 mmol) in DMF (250 ml) was treated with Na2CO3 (10.6 g; 0.1 mol) and the mixture was stirred at room temperature for 3 days. The mixture was poured into water and extracted with Et2O. The organic phase was washed with brine and dried over MgSO4. The residue was purified by flash chromatography eluting with CH2Cl2 to give 5-benzyloxy-2-chloro-nitrobenzene as a pale yellow solid (12.32 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030123B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-c72694a60dbf44c58f87db05f0258986 |
| Source note | uspto-grants-2006_04 |