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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749242Generated: October 31, 2026

(R)-2-Methyl-CBS-oxazaborolidine → 4-(Benzyloxy)-7-[(1R)-2-bromo-1-hydroxyethyl]-1,3-benzothiazol-2(3H)-one

https://huagongshe.com/reaction/749242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant4-(Benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-oneHCID 85939637—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzyloxy)-7-[(1R)-2-bromo-1-hydroxyethyl]-1,3-benzothiazol-2(3H)-oneHCID 6892657069.8%

Reaction Steps

A solution of [(R)-tetrahyro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo[1,2-c] [1,3,2]-oxazaborole] (22 μl of 1M in toluene) in dry THF(1 ml) was cooled to −5° C., stirring under nitrogen. Borane-methyl sulfide complex (2M solution in THF, 11 μl) was added and stirred for 10 min at −5° C. A solution of 4-(benzyloxy)-7-(bromoacetyl)-1,3-benzothiazol-2(3H)-one (47 mg) in dry THF (1.5 ml) was added dropwise and then another 66 μl of borane-methyl sulfide complex (2M solution in THF). The reaction mixture was left for 72 h at less than 5° C. and then partitioned between 2N HCl and ethyl acetate. The organic solution was dried (MgSO4), filtered and evaporated in vacuo. The residue was purified on a 5 g silica SPE cartridge, eluting with a stepped gradient of 10% to 25% ethyl acetate-cyclohexane mixtures to give the title compound (33 mg). LCMC RT=3.19 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402598B2
Source datasetuspto-grants-2008_07
ORD IDord-ce280e62366e4937bcc9a4de957cd692
Source noteuspto-grants-2008_07