HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Xylyl bromide → HCID 66918677, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | HCID 66918607 | HCID 66918607 | — |
| Catalyst | HCID 178418778 | HCID 178418778 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66918677 | HCID 66918677 | 59.3% |
Reaction Steps
A mixture of (1R,2R,4R) and (1S,2S,4S)-4-(2-chloro-benzenesulfonyl)-2-hydroxy-cyclopentanecarboxylic acid methyl ester (80 mg, 0.251 mmol, example 48, step 5), 1-(bromomethyl)-4-methylbenzene (232 mg, 1.25 mmol) and silver(I) oxide (116 mg, 0.502 mmol) in DCM (2 ml) was stirred at room temperature for 60 h. The reaction mixture was filtered through a pad of Celite, the pad was washed with DCM and the filtrate was evaporated. The remaining grey oil was purified by silica gel chromatography (heptane/EtOAc 80:20-70:30) to obtain the title compound (63 mg, 56%) as colorless oil. MS (EI): 423.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893099B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-fb2c74bd01a64c1c9be943a5e408eeb8 |
| Source note | uspto-grants-2011_02 |