HuagongsheHuagongshe Chemistry Print Report · For research reference only
Myristyl bromide → (1,1-Difluoro-pentadecyl)Phosphonic Acid Diethyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Myristyl bromide | HCID 8208 | — |
| Reactant | Phosphonic acid, (difluoromethyl)-, diethyl ester | HCID 2758305 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1,1-Difluoro-pentadecyl)Phosphonic Acid Diethyl Ester | HCID 11773544 | 40% |
Reaction Steps
To a solution of diethyl difluoromethanephosphonate (1.0 g, 5.316 mmol) in THF (50 mL) 2 M LDA (626 mg, 5.847 mmol) was added at −78° C. and stirred for 30 min. Tetradecyl bromide (1.474 g, 5.316 mmol) in THF (10 mL) was added to the mixture at −78° C. and the reaction mixture was stirred overnight. THF was evaporated and the residual oil was purified by flash chromatography using 30% ethyl acetate in hexane as eluent to give 817 mg (40%) of compound 10 as colorless oil. 1H NMR (CDCl3): δ4.26 (m, 4H), 2.05 (m, 2H), 1.56 (m, 2H), 1.37 (t, J=6.9 Hz, 6H), 1.25 (br s, 22H), 0.87 (t, J=6.6 Hz, 3H); MS: [M+23Na] at m/z 407.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947665B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-4117f5ade5304ceeb2b3ea1da2f2567e |
| Source note | uspto-grants-2011_05 |