HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Diisopropyl hydroxymethylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorous acid, bis(1-methylethyl) ester | HCID 21884976 | — |
| Product | Diisopropyl hydroxymethylphosphonate | HCID 10867235 | 91% |
Reaction Steps
A mixture of 33.2 g (0.20 mol) of diisopropyl phosphite, 2.8 mL (0.02 mol) of triethylamine, and 6.0 g (0.20 mol) of paraformaldehyde, was immersed in a 100° C. oil bath and then heated between 100°-120° C. for 45 minutes under nitrogen. An exotherm occurred within 10 minutes and all of the paraformaldehyde dissolved rapidly. The triethylamine was removed at reduced pressure, and the residue was bulb-to-bulb distilled in four portions to provide a total of 35.17 g (91%) of title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278153 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-bd721dbe4e5741b6ac44356a182c9346 |
| Source note | uspto-grants-1994_01 |