HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → (3S)-1-bromo-4-(4-fluorophenoxy)-3-hydroxy-1-butyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Butyn-2-ol, 1-(4-fluorophenoxy)-, (2S)- | HCID 86588775 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | (3S)-1-bromo-4-(4-fluorophenoxy)-3-hydroxy-1-butyne | HCID 67096607 | — |
Reaction Steps
A mixture of (3S)-4-(4-fluorophenoxy)-3-hydroxy-1-butyne (2.5 g, 14 mmol), N-bromosuccinimide (NBS) (2.74 g, 15.4 mmol) and AgNO3 (0.12 g, 0.7 mmol) in acetone (70 mL) was stirred at ambient temperature. The pale solution became cloudy over 30 minutes. The mixture was concentrated under vacuum and the resulting residue was filtered through a plug of silica gel (1×5 cm) eluted with 1:4 ethyl acetate:hexane to obtain (3S)-1-bromo-4-(4-fluorophenoxy)-3-hydroxy-1-butyne, a compound of formula (CC), as a pale yellow oil containing some ethyl acetate, 4.75 g (quant.); 1H NMR (CDCl3) δ 3.95-4.15 (m, 2H), 4.75 (m, 1H), 6.86 (m, 2H), 6.97 (m, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928255B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-4adbec656b1a4be2a2fd435be757d52f |
| Source note | uspto-grants-2011_04 |