HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161764Generated: October 29, 2026
Benzyl Bromide → 4-(Benzyloxy)-2,6-dichlorobenzaldehyde
https://huagongshe.com/reaction/1161764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dichloro-4-hydroxybenzaldehyde | HCID 528382 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Benzyloxy)-2,6-dichlorobenzaldehyde | HCID 11150210 | — |
Reaction Steps
Treat a mixture of 2,6-dichloro-4-hydroxy-benzaldehyde (250 g, 1.3 mol) and potassium carbonate (361.8 g, 2.62 mol) in 2 L dimethylformamide with benzyl bromide (268.64 g, 1.57 mol). Stir the reaction at room temperature for 1 hour. Filter off solids and pour into 12 L of water. Filter off solid, wash several times with water, air dry and dissolve in ethyl acetate. Dry over magnesium sulfate, filter and concentrate under vacuum to ˜1.5 L. Allow to sit overnight then filter. Wash solid with minimal amount of hexane and vacuum dry. Concentrate the filtrate under vacuum and triturate with hexane to yield a second crop of product which when combined with the first crop equals 245 g white crystals. Repeat to obtain a 3rd crop of 80 g as a light-tan powder (88% overall yield): 1H NMR (400 MHz, DMSO-d6) δ 10.26 (s, 1H), 7.43 (m, 5H), 7.28 (s, 2H), 5.25 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07820659B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-739837224d77445ea27e53b00e05b325 |
|---|
| Source note | uspto-grants-2010_10 |
|---|