HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572498Generated: October 31, 2026
HCID 68294906, compound → HCID 68295247, compound
https://huagongshe.com/reaction/572498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 68294906 | HCID 68294906 | — |
| Reactant | HCID 68294936 | HCID 68294936 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68295247 | HCID 68295247 | 88.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029391B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-6f39df1367a8400f83013f084c94183e |
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| Source note | uspto-grants-2015_05 |
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