HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 57779447, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Ethyl bromophenylacetate | HCID 97780 | — |
| Reactant | Sodium Ascorbate | HCID 23667548 | — |
| Reactant | HCID 86632440 | HCID 86632440 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 57779447 | HCID 57779447 | 65% |
Reaction Steps
To a solution of ethyl 2-bromo-2-phenylacetate 21 (1.60 g, 6.58 mmol) in sodium azide/DMSO solution (0.5 M, 13.16 mL, 6.58 mmol) which had been stirred at room temperature for 1 h was added water (10 mL), sodium ascorbate (0.130 g, 0.658 mmol), phenylacetylene (0.723 mL, 6.58 mmol) and aq. copper(II) sulfate solution (1.0 M, 1.30 mL, 1.30 mmol) (in that order). The reaction mixture was stirred for 16 h. Brine was added and extraction with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated. The crude material was purified by silica gel column chromatography with gradient of ethyl acetate (0-50%) in hexane to afford compound (24) as a light yellow solid (1.31 g, 65%). LRMS: calc. 307.4, found 308.4 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096565B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-46c1157c478b41429391923266b8c5aa |
| Source note | uspto-grants-2015_08 |