HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → 4-(2-hydroxyethoxy)-3-methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-hydroxyethoxy)-3-methoxybenzaldehyde | HCID 3152712 | — |
Reaction Steps
Vanillin (15.2 g, 0.01 m), water (70 mL), and sodium hydroxide (5.0 g, 0.0125 m) are mixed and stirred for a few minutes until solution is completed. 2-Chloroethanol (9.7 g, 0.012 m) is added and the reaction mixture heated at reflux for 16 hours and then cooled. The solid product is collected by filtration, washed with water, dried, and finally recrystallized from toluene. The yield is 13.0 g (69.9% of the theoretical yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04707537 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-17fecfb0abf44957a35b62f0cac01ca7 |
| Source note | uspto-grants-1987_11 |