Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212073Generated: November 1, 2026

HCID 69663378, compound → HCID 69662332, compound

https://huagongshe.com/reaction/2212073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69663378HCID 69663378—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69662332HCID 69662332—

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium in hexanes (0.165 ml, 0.25 mmol) was added dropwise to a stirred solution of (3R*,4R*)-4-benzenesulfonyl-3-methylpentan-1-ol (286 mg, 1.2 mmol) in THF (5 ml) at −78° C. The mixture was warmed to 0° C. over 30 min. and quenched with satd. aqueous NH4Cl and extracted with dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated to give a mixture syn:anti diastereoisomeric sulfones in a 6:1 ratio respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101892B2
Source datasetuspto-grants-2006_09
ORD IDord-ea53e607d5964a968dfb66debd969106
Source noteuspto-grants-2006_09