HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1,3-Dichloro-5-ethynylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | [2-(3,5-Dichlorophenyl)ethynyl]trimethylsilane | HCID 22570337 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,3-Dichloro-5-ethynylbenzene | HCID 13823547 | — |
Reaction Steps
To a solution of (3,5-dichloro-phenylethynyl)-trimethylsilane (4.85 g, 19.9 mmol) in methanol (50 mL) was added 1M potassium hydroxide (30 mL). The reaction mixture was stirred 1 h at room temperature and evaporated. The residue was treated with water (10 mL) and extracted with 3×40 mL diethyl ether. The tried organic phases were evaporated to give the desired 1,3-dichloro-5-ethynyl-benzene product in 2.3 g yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06569901B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-af94009c5e254f698fc70f31fcd57cb7 |
| Source note | uspto-grants-2003_05 |