HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Benzoylbenzaldehyde → HCID 13102753, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Benzoylbenzaldehyde | HCID 13020168 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13102753 | HCID 13102753 | — |
Reaction Steps
Ethynylmagnesium bromide (11.2 mmol) in tetrahydrofuran (20 cm3) was added dropwise to a stirred solution of 3-benzoylbenzaldehyde (2 g, 9.5 mmol, prepared as in Example 3(b) in tetrahydrofuran (30 cm3) through which purified acetylene was being passed. After 2 hours, saturated ammonium chloride solution (200 cm3) was added, and the mixture extracted with ether (3×50 cm3). The combined extracts were washed with saturated sodium chloride, dried over anhydrous sodium sulphate, and the solvent removed in vacuo. The product was purified by thin layer chromatography on silica to give the title alcohol, yield 1.1 g (49%) nD20 1.6075.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504491 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-b6af8858aa2d42aeb42065e78db42027 |
| Source note | uspto-grants-1985_03 |