HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 54474351, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 54176324 | HCID 54176324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54474351 | HCID 54474351 | 76% |
Reaction Steps
A solution of 3-(5-bromo-3-pyridinyl)prop-2-en-1-ol (0.85 gms, 3.97 mmol) is diluted with methylene chloride (20 mls). Thionyl chloride (0.27 mls, 97%, leq) is added at room temperature. After one hour a second equivalent of thionyl chloride is added. The reaction is neutralized with saturated aqueous NaHCO3 after an additional hour and extracted with methylene chloride. The organic layer is dried over Na2SO4 and evaporated to yield 0.70 gms of an oil (76%). 1H NMR (CDCl3, 300 MHz) δ8.90 (s, 1H), 8.70 (s, 1H), 8.40 (s, 1H), 6.70 (m, 2H), and 4.30 (d, J=3.8 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05191084 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-80e53a67765e4f8389401ce325afa588 |
| Source note | uspto-grants-1993_03 |