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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047440Generated: October 31, 2026

Hexane → HCID 86636115, compound

https://huagongshe.com/reaction/1047440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant7-Chlorothieno[3,2-b]pyridineHCID 11275251—
ReactantHCID 57967257HCID 57967257—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86636115HCID 8663611550%

Reaction Steps

A solution of 7-chlorothieno[3,2-b]pyridine (6) (4.49 g, 26.6 mmol) in THF (20 ml) was treated with 2.5 M hexane solution of n-BuLi (11.1 mL, 27.9 mmol) at −78° C. and allowed to stir at the same temperature for 45 min. The reaction mixture was then treated with 1M ether solution of ZnCl2 (28 mL, 28 mmol) and stirred at room temperature for an additional 1 h. The reaction mixture was then treated with 56 (2.3 g, 6.7 mmol) and Pd(PPh3)4 and was heated to reflux for 2 hrs. It was quenched with saturated NaHCO3 (50 mL) and extracted with EtOAc (2×50 mL). The extract was dried over anhydrous Na2SO4, filtered and evaporated. Obtained crude product was purified by flash chromatography (using the gradient 60-80% EtOAc/hexanes as an eluent), yielding 57 (1.43 g, 50% yield). MS (m/z): 434.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569503B2
Source datasetuspto-grants-2013_10
ORD IDord-ebe501ed109945038e065df8230922e4
Source noteuspto-grants-2013_10