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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655632Generated: November 2, 2026

Thionyl Chloride → HCID 54474351, compound

https://huagongshe.com/reaction/1655632

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) δ 8.90 (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 numberUS05250700
Source datasetuspto-grants-1993_10
ORD IDord-9a4234c13743457b903c9f5ab07f55c4
Source noteuspto-grants-1993_10