HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl (diphenoxyphosphoryl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | Diphenoxyphosphanolate | HCID 23418553 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl (diphenoxyphosphoryl)acetate | HCID 10689048 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of diphenylphosphite (2.25 mL) in dichloromethane at 0° C. was added t-butylbromoacetate (1.48 mL) followed by triethylamine (1.95 mL). The mixture was stirred at 0° C. for 15 min and then at rt for 1 h before being quenched with water and extracted into ethyl acetate, dried over MgSO4 and concentrated. The residue was purified by silica gel chromatography eluting with hexane/ethyl acetate to give the title compound. 1H NMR (500 MHz, CDCl3): δ 7.40-7.18 (m, 10H); 3.22 (s, 1H); 3.18 (s, 1H); 1.50 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809199B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-65ac710e789949a5880f74f2b654d1e1 |
| Source note | uspto-grants-2004_10 |