HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67451842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67452000 | HCID 67452000 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67451842 | HCID 67451842 | 93.4% |
Reaction Steps
To a solution of 5-[(4-chlorophenyl)sulfanyl]-2-(tetrahydro-2H-pyran-4-yl)-1,3-oxazole (521 g, 17.61 mmol) in DCM (176 ml) was added NBS (3.45 g, 19.38 mmol) and the reaction mixture was stirred at RT for 16 h. The reaction mixture was concentrated in vacuo and purified by flash chromatography (silica 330 g, 5 to 30% EtOAc in hexane), to give 4-bromo-5-[(4-chlorophenyl)sulfanyl]-2-(tetrahydro-2 H-pyran-4-yl)-1,3-oxazole (6.16 g). MS: M+H=376. H′NMR (400 MHz, CDCl3) δ: 7.28 (d, J=8.4 Hz, 2 H), 7.22 (d, J=8.4 Hz, 2 H), 4.01 (dt, J=11.7 Hz, 3.6 Hz, 2 H), 3.50 (td, J=2.7, 11.7 Hz, 2 H), 3.09-2.98 (m, 1 H), 2.02-1.86 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193697B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-67a9733236074727a279e9aa611e5d45 |
| Source note | uspto-grants-2015_11 |