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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879260Generated: October 30, 2026

(R)-2-Methyl-CBS-oxazaborolidine → (S)-ethyl 2-(2-bromo-5-methyl-7-(trifluoromethylsulfonyloxy)benzo[d]thiazol-6-yl)-2-hydroxyacetate

https://huagongshe.com/reaction/879260

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
ReactantEthyl 2-(2-bromo-5-methyl-7-(trifluoromethylsulfonyloxy)benzo[d]thiazol-6-yl)-2-oxoacetateHCID 86699782—
SolventTolueneHCID 1140—
Product(S)-ethyl 2-(2-bromo-5-methyl-7-(trifluoromethylsulfonyloxy)benzo[d]thiazol-6-yl)-2-hydroxyacetateHCID 86699783—

Reaction Conditions

Temperature-35 °C

Reaction Steps

To a solution of 30 (8.30 g, 17.4 mmol) in toluene (70 mL) was added ((R)-2-methyl-CBS-oxazaborolidine (725 mg, 2.61 mmol). The reaction mixture was then cooled to −35° C. and a solution of catecholborane (freshly distilled) (1 M in toluene, 20.9 mL, 20.9 mmol) was added via addition funnel over 30 min. The reaction was stirred for 20 min while warming to −20° C. A 2 M solution of Na2CO3 was added (50 mL). The layers were separated, and the organic layer was washed with additional Na2CO3 solution (3×25 mL). The organic layer was dried, filtered, and concentrated in vacuo to give 31, which had analytical data to match 29. The compound was taken on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-6ed3ac39bdf2428fbd8f4a9a43b4e04e
Source noteuspto-grants-2015_03