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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245506Generated: October 31, 2026

Boron trifluoride → {7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazol-5-yl}methanol

https://huagongshe.com/reaction/245506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantSodium borohydrideHCID 4311764—
ReactantDiboronHCID 6328200—
Reactant7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazole-5-carboxylic acidHCID 67357238—
SolventTetrahydrofuranHCID 8028—
SolventDiglymeHCID 8150—
Product{7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazol-5-yl}methanolHCID 67356497—

Reaction Steps

To a stirred solution of NaBH4 (78 mg, 2.43 mmol) in diglyme (1 mL) was added BF3 (1.6 mL, 2.59 mmol), and the thus generated diborane gas was purged into solution of 7-chloro-6-[(2R,6S)-2,6-dimethylmorpholin-4-yl]-3-methyl-1,2-benzoxazole-5-carboxylic acid (Intermediate 302, 250 mg, 0.8 mmol) in THF (1 mL). The mixture was stirred at room temperature for 30 minutes before being quenched with methanol (1 mL) and concentrated. The residue was purified by column chromatography to give product as solid. Yield: 130 mg (52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658641B2
Source datasetuspto-grants-2014_02
ORD IDord-c6dcf7c953e5453cb9a0719b9b717f07
Source noteuspto-grants-2014_02