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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275631Generated: November 1, 2026

Lithium tri-s-butylborohydride → HCID 66661829, compound

https://huagongshe.com/reaction/2275631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium tri-s-butylborohydrideHCID 3611392—
ReactantHCID 66662325HCID 66662325—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66661829HCID 6666182960.1%

Reaction Steps

To a solution of benzyl 3-oxo-4-phenylpyrrolidine-1-carboxylate (200 mg, 0.0007 mol) in tetrahydrofuran (2.0 mL, 0.025 mol) under a N2 atmosphere at −78° C. was added L-Selectride® in tetrahydrofuran (1M, 4.1 mL) with stirring. The mixture was stifled at this temperature for 1.5 hours. LCMS indicated that the starting material was consumed and the reaction was quenched with water. The solution was adjusted to pH ˜6 to 7 and was extracted with EtOAc. The organic extract was washed with brine, dried over Na2SO4, filtered and the filtrate was concentrated. The resulting residue was purified with Combiflash, eluting with EtOAc/hexane to afford the product (125 mg). LCMS: m/z 298.0 (M+H+); 320.0 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126927B2
Source datasetuspto-grants-2015_09
ORD IDord-1b443e4f32a54b65a569b5e4f53eeb9d
Source noteuspto-grants-2015_09