HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 22270422, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2,3-bis(4-chlorophenyl)propionate | HCID 22270406 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | HCID 22270422 | HCID 22270422 | — |
Reaction Steps
To a solution of methyl 2,3-bis(4-chlorophenyl)propionate (2.6 g, 8.4 mmol) in ether (20 mL) was added methylmagnesium bromide (3 M in ether, 8.4 mL, 25 mmol) at −10° C., and the reaction was allowed to warm to room temperature over 2 h. The reaction mixture was poured into saturated aqueous ammonium chloride (100 mL), and the product was extracted with EtOAc (3×100 mL). The combined extracts were dried over anhydrous MgSO4, filtered, and concentrated to dryness to give the title compound, which was used without further purification. 1H NMR (500 MHz, CD3OD): δ 7.17 (ABq, 4H), 7.06 (d, 2H), 6.93 (d, 2H), 3.32 (dd, 1H), 2.94 (dd, 1H), 2.84 (dd, 1H), 1.20 (s, 3H), 1.16 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06972295B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-ea653caddf8d470189d276f3533be152 |
| Source note | uspto-grants-2005_12 |