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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634859Generated: October 30, 2026

Phosphorus tribromide → HCID 22006938, compound

https://huagongshe.com/reaction/634859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus tribromideHCID 24614—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22006939HCID 22006939—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22006938HCID 2200693834.9%

Reaction Steps

To a stirred solution of 3.4 grams (0.019 mole) of (2-ethylbenzoxazol-5-yl)methanol in 25 mL of toluene was added 1.6 grams (0.006 mole) of phosphorous tribromide from a syringe. A precipitate formed immediately, and additional toluene was added to the reaction mixture to aid stirring. The reaction caused the reaction mixture temperature to rise to about 35° C. Upon completion of the addition, the reaction mixture stirred for an additional 20 minutes. The reaction mixture was then concentrated under reduced pressure to a residual solid. The solid was dissolved in 30 mL of dimethyl sulfoxide and, with stirring, 3.7 grams (0.029 mole) of N,N-diisopropylethylamine and 3.1 grams (0.019 mole) of ethyl piperdin-4-ylcarboxylate were added simultaneously from syringes. The resultant reaction caused the reaction mixture temperature to rise to about 40° C. The reaction mixture was allowed to cool to ambient temperature as it stirred for about 18 hours. The reaction mixture was poured into water and extracted with ethyl acetate and then with diethyl ether. The combined extracts were washed with an aqueous solution saturated with sodium bicarbonate, and then with an aqueous solution saturated with sodium chloride. The organic layer was concentrated under reduced pressure to a residual oil, which was subjected to column chromatography on silica gel, with ethyl acetate as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 2.1 grams of ethyl N-(2-ethylbenzoxazol-5-ylmethyl)piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184234B2
Source datasetuspto-grants-2001_02
ORD IDord-131c70d9e9564b5db3b22885323aad90
Source noteuspto-grants-2001_02