HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4S)-4-(propan-2-yl)-1,3-oxazolidin-2-one → HCID 178446066, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4S)-4-(propan-2-yl)-1,3-oxazolidin-2-one | HCID 7157133 | — |
| Reactant | HCID 28564749 | HCID 28564749 | — |
| Reactant | HCID 53738541 | HCID 53738541 | — |
| Product | HCID 178446066 | HCID 178446066 | — |
Reaction Steps
4(S)-(1-Methylethyl)-3-{1-oxo-3-[1-(triphenylmethyl)-1H-imidazol-4-yl]propyl}-2-oxazolidinone: By following the procedure of example 2, section (b) and using the product of section (a) of this example (11.5 g, 30.1 mmol) to prepare the corresponding mixed anhydride which in turn is reacted with the (S)-4-(1-methylethyl)-2-oxazolidinone (3.53 g, 27.3 mmol), the desired product was obtained as a pale yellow solid (11.38 g, 84%); 1H NMR(CDCl3) δ7.36-7.29 (m,10H), 7.17-7.10 (m,6H), 6.58 (d, J=0.7 Hz,1H), 4.40 (td, J=3.8 Hz, 7.5 Hz,1H), 4.29-4.14 (m,2H), 3.32-3.23 (m,2H), 2.96-2.88 (m,2H), 2.33 (hept d, J=3.8 Hz, 6.9 Hz, 1H), 0.89 (d, J=7.0 Hz, 3H), 0.82 (d, J=6.9 Hz,3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541163 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-b8ab150ad8b04ca7bc6c6767972aed12 |
| Source note | uspto-grants-1996_07 |