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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444283Generated: October 31, 2026

Hexane → HCID 178522032, compound

https://huagongshe.com/reaction/1444283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium HydroxideHCID 14798—
ReactantAzido(trimethyl)stannaneHCID 5104973—
ReactantHCID 59654780HCID 59654780—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 178522032HCID 178522032—

Reaction Steps

To a solution of 5-phenyl-furan-2-carboxylic acid (3-cyanomethyl-phenyl)-amide (70 mg, 0.23 mmol) in toluene (3 ml) was added Me3SnN3 (56 mg, 0.28 mmol). After heating to reflux for 18 h, additional Me3SnN3 (56 mg, 0.28 mmol) and toluene (2 ml) were added and the reaction was heated to reflux for a further 18 h. After this time, 2M NaOH (2 ml) and hexane (2 ml) were added to the reaction mixture and stirred for 10 min. Water (1 ml) was added and the organic layer separated. EtOAc (2 ml) was added to the aqueous layer and the solution stirred for 2 min before the organic layer was separated. The combined organic layers were discarded. The aqueous layer was then acidified to pH 5 with 2M HCl then EtOAc (2.5 ml) was added and the solution stirred for 10 min after which time the organic layer was separated. EtOAc (2.5 ml) was added to the aqueous layer and the solution stirred for 1 hour. The EtOAc layer was separated and these combined organic layers were evaporated in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662839B2
Source datasetuspto-grants-2010_02
ORD IDord-adc8fa626b624ac98bdc2c7b4d3abc04
Source noteuspto-grants-2010_02