HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360952Generated: October 27, 2026
Benzyl Chloride → 3-(Benzyloxy)-4-ethoxybenzaldehyde
https://huagongshe.com/reaction/2360952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Ethoxy-3-hydroxybenzaldehyde | HCID 75679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Benzyloxy)-4-ethoxybenzaldehyde | HCID 818573 | 83.9% |
Reaction Steps
16.6 grams of 4-ethoxy-3-hydroxybenzaldehyde (100 mmol.) and 200 ml of absolute ethyl alcohol are added to a three-necked flask and then heated to 40° C. for being dissolved, 9 grams of potassium carbonate (65.07 mmol.) is added, 15 ml of benzyl chloride (130.13 mmol.) is added under stirring, heating reflux is performed for 1 hour, the reaction product is cooled to 50° C. after complete reaction is detected by TLC and then filtered while it is hot, the filtrate is put in a refrigerator for being cooled over night, crystals are separated out and pump-filtered, filter cakes are washed with 30 mL of absolute ethyl alcohol and then vacuum-dried to obtain 21.5 grams of white needle crystals, and the yield is 83.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08686187B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-2f05b01c0e674fc6908fbae147c78e01 |
|---|
| Source note | uspto-grants-2014_04 |
|---|