Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612948Generated: October 30, 2026

Thionyl Chloride → HCID 54474351, compound

https://huagongshe.com/reaction/1612948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 54176324HCID 54176324—
SolventDichloromethaneHCID 6344—
ProductHCID 54474351HCID 5447435176%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05191084
Source datasetuspto-grants-1993_03
ORD IDord-80e53a67765e4f8389401ce325afa588
Source noteuspto-grants-1993_03