Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301165Generated: October 31, 2026

(R)-2-Methyl-CBS-oxazaborolidine → HCID 54202943, compound

https://huagongshe.com/reaction/2301165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54202943HCID 5420294381%

Reaction Steps

A solution of 2.7 mL of 1.0 M (R)-2-methyl-CBS-oxazaborolidine solution in toluene in 4 mL of CH2Cl2 at −25° C. was treated with 1.4 mL of 2.0 M borane methyl sulfide complex in THF and stirred cold for 10 min. A solution of 501 mg (2.66 mmol) of cyclopentylmethylene phenyl ketone (from Step B) in 2 mL of CH2Cl2 was added over 25 min and the resulting mixture was stirred cold for an additional 45 min. The reaction was quenched by pouring it into cold (−25° C.) MeOH. The quenched reaction was warmed to rt and stirred for 45 min until gas evolution ceased. The mixture was concentrated and the residue dissolved in 20 mL of MeOH and concentrated again. Flash chromatography on silica gel using 17:3 v/v hexanes/EtOAc afforded 413 mg (81%) of the title compound: RF: 0.53 (4:1 v/v hexanes/ EtOAc); 1H NMR (300 MHz): δ 1.10-1.17 (m, 2H), 1.47-1.89 (m, 9H), 4.69 (m, 1H), 7.25-7.35 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498161B1
Source datasetuspto-grants-2002_12
ORD IDord-9d0c69bc85fc4626bc0158e032eb73f8
Source noteuspto-grants-2002_12