HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → HCID 53973893, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Allyl-4-hydroxybenzaldehyde | HCID 4729014 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 53973893 | HCID 53973893 | — |
Reaction Steps
1,3-Dibromopropane (15.76 ml) and potassium carbonate (4.69 g) were added to a solution of 3-allyl-4-hydroxybenzaldehyde (5 g) in acetone and the reaction mixture heated at reflux for 16 hours. The reaction mixture was cooled to ambient temperature and filtered. The filtrate was evaporated and the residue purified by flash column chromatography on silica gel (Merck Art No 9385) using a 10:90 (v/v) mixture of ethyl acetate/hexane as eluent to give 3-allyl-4-(3-bromopropoxy)benzaldehyde (4.86 g) as an oil which slowly solidified. NMR([CD3 ]2SO): 2.2-2.4(2H,m), 3.35-3.50(2H,m), 3.65-3.80(2H,t), 4.2-4.3(2H,t), 5.0-5.15(2H,m), 5.8-6.1(1H,m), 7.15-7.25(1H,d), 7.7(1H,d), 7.75-7.85(1H,q) and 9,85(1H,s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866611 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-84219d9be37a442fa1ce8c6e3c548024 |
| Source note | uspto-grants-1999_02 |