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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040443Generated: October 31, 2026

Pentane → HCID 57517878, compound

https://huagongshe.com/reaction/2040443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-BromomesityleneHCID 68473—
Reactant2-MethoxypyridineHCID 74201—
Reactant5-IodoisatinHCID 88695—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57517878HCID 5751787850.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 1.7 M solution of tert-butyllithium in pentane (35 ml, 60 mmol) was added to THF (100 ml) at −78° C. 2-Bromomesitylene (4.6 ml, 30 mmol) was added dropwise and the mixture stirred at −78° C. for 1 h. 2-Methoxypyridine (3.2 ml, 30 mmol) was added at −78° C. and then the mixture was stirred at 0° C. for 1.5 h. The ice-cold solution of the lithiated 2-methoxypyridine was transferred (via a transfer needle) into an ice-cold suspension of 5-iodoisatin (4.1 g, 15 mmol) in THF (150 ml). The reaction mixture was allowed to warm to room temperature and then saturated ammonium chloride solution was added. The mixture was extracted three times with ethyl acetate, and the collected extracts were washed with saturated brine. The organic phase was dried over magnesium sulfate, filtered and concentrated under reduced pressure. Purification by crystallization from dichloromethane yielded 2.9 g of the intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580842B2
Source datasetuspto-grants-2013_11
ORD IDord-ca23f3e1ba8d4bb186a554c0da24884e
Source noteuspto-grants-2013_11