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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602091Generated: October 30, 2026

Hexane → HCID 9906375, compound

https://huagongshe.com/reaction/1602091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Reactant4-Methylthiomorpholin-3-oneHCID 13606349—
ReactantButyllithiumHCID 178418339—
CatalystSilver(II) oxideHCID 92152—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9906375HCID 990637540%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-methyl-3-thiomorpholinone (1.88 g, 14.3 mmol) dissolved in tetrahydrofuran (72 ml) was cooled to 0° C. and treated with 1.37M n-butyl lithium in hexane (20.9 ml, 28.7 mmol). After five minutes, the cold bath was removed. Ten minutes later a solution of 2,6-di-t-butyl-quinone methide, prepared by adding silver oxide (33.2 g, 143 mmol) to 2,6-di-t-butyl-4-methyl-phenol (BHT) (3.16 g, 14.3 mmol) in tetrahydrofuran (72 ml) stirring for 30 minutes and filtering, was added dropwise over 20 min. The reaction was stirred for three hours, quenched with 1N hydrochloric acid, and evaporated to an aqueous suspension. The crude product was extracted into ethyl acetate, dried over sodium sulfate and concentrated in vacuo. Chromatography on silica gel eluting with 8 L of a 0-50% ethyl acetate in hexane gradient yielded desired product (2.0 g, 40%):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981523
Source datasetuspto-grants-1999_11
ORD IDord-b5c17593911041f0b24943f1e1a82018
Source noteuspto-grants-1999_11