HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicyl Alcohol → Diethyl 2-hydroxybenzylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicyl Alcohol | HCID 5146 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Diethyl 2-hydroxybenzylphosphonate | HCID 23415580 | 90% |
Reaction Steps
38.4 g of 2-hydroxybenzylalcohol from TOKYO KASEI KOGYO Co., Ltd. and 80 ml of o-xylene were put in a reaction reservoir having a mixer, a thermometer and a dropping funnel. Under a nitrogen stream, 62.8 g of triethyl phosphite were slowly dropped therein at 80° C., and the reaction therein is further performed for 1 hr at the same temperature. Then, the produced ethanol, o-xylene and unreacted triethyl phosphite were removed from the reaction by reduced-pressure distillation to prepare 66 g of 2-diethylhydroxybenzylphosphonate at a yield of 90%, having a boiling point of 120.0° C./1.5 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114563B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-1882de1003c64074820bd835c4dc21df |
| Source note | uspto-grants-2012_02 |