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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-2-Methyl-CBS-oxazaborolidine | HCID 9838490 | — |
| Reactant | Ethyl 2-(2-bromo-5-methyl-7-(trifluoromethylsulfonyloxy)benzo[d]thiazol-6-yl)-2-oxoacetate | HCID 86699782 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (S)-ethyl 2-(2-bromo-5-methyl-7-(trifluoromethylsulfonyloxy)benzo[d]thiazol-6-yl)-2-hydroxyacetate | HCID 86699783 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987250B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-6ed3ac39bdf2428fbd8f4a9a43b4e04e |
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| Source note | uspto-grants-2015_03 |
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