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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432883Generated: October 31, 2026

Sodium Iodide → HCID 53788388, compound

https://huagongshe.com/reaction/1432883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAllyl AlcoholHCID 7858—
Reactant2-Bromo-5-chlorothiopheneHCID 76133—
ReactantSodium BicarbonateHCID 516892—
Catalystpalladium(II) acetateHCID 167845—
SolventDiethyl EtherHCID 3283—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 53788388HCID 5378838820.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of Pd(OAc)2 (0.12 g, 0.53 mmol), NaHCO3 (0.52 g, 6.19 mmol) and NaI (0.28 g, 1.87 mmol) in 5 mL of HMPA is added 5-bromo-2-chloro-thiophene (1.00 g, 5.06 mmol) and allyl alcohol (1.03 mL, 15.2 mmol). The mixture is heated to 90° C. and stirred for 16 hours. The reaction mixture is cooled to room temperature, diluted with Et2O and washed with water. The organic layer is dried over MgSO4, filtered and concentrated in vacuo. The crude residue is purified by flash column chromatography eluting with a gradient of 10% Et2O/hexanes to 20% Et2O/hexanes to provide the product (0.18 g, 1.03 mmol) as an oil. 1H NMR (CDCl3, 300 MHz) δ9.81 (s, 1H), 6.71 (d, 1H), 6.58 (d, 1H), 3.07 (t, 2H), 2.81 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-3a62767deb3a4916a6a8a10d3e00875f
Source noteuspto-grants-2009_11