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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572498Generated: October 31, 2026

HCID 68294906, compound → HCID 68295247, compound

https://huagongshe.com/reaction/572498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68294906HCID 68294906—
ReactantHCID 68294936HCID 68294936—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68295247HCID 6829524788.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

An ice cooled suspension of 2-((8-fluoro-5-methylchroman-6-yl)methyl)-N-methylbenzamide (300 mg, 0.957 mmol) in THF (5 mL) was treated with 2.5M nBuLi in hexanes (804 μl, 2.010 mmol). Upon addition of the n-BuLi, the reaction became homogeneous and dark red in color. After 10 min, a solution of (2S)-5,6-dimethoxy-5,6-dimethyl-1,4-dioxane-2-carbonitrile (289 mg, 1.436 mmol) in THF (0.5 mL) was added and the colorless solution was maintained at 0° C. for 5 min. The reaction was quenched with sat. aq. NH4Cl and extracted with EtOAc. The combined organics were washed with brine, dried (Na2SO4), filtered and concentrated. The residue was purified by ISCO (0-10% MeOH-DCM) to afford the title compound (408 mg, 0.844 mmol, 88% yield) as a 1:1 mixture of diastereomers as a pale yellow foam. LC/MS (m/z) ES+=484 (M+1). Rt=2.17, 2.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029391B2
Source datasetuspto-grants-2015_05
ORD IDord-6f39df1367a8400f83013f084c94183e
Source noteuspto-grants-2015_05