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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304408Generated: November 1, 2026

Benzoic Acid → (+)-5-[[(2R, 4S)-4-benzoyloxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepine

https://huagongshe.com/reaction/2304408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(+)-5,11-dihydro-5-[[(2R,4R)-4-hydroxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]dibenzo[b,e][1,4]oxazepineHCID 15481939—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(+)-5-[[(2R, 4S)-4-benzoyloxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepineHCID 1548194183.3%

Reaction Steps

Mixture of 660 mg (1.53 mmol) of (+)-5,11-dihydro-5-[[(2R, 4R) -4-hydroxy-1-(4-methoxyphenethyl) pyrrolidin-2-yl]methyl]dibenzo[b,e][1,4]oxazepine, 1.04 g (3.98 mmol), 486 mg (3.98 mmol) of benzoic acid, and 693 mg (3.98 mmol) of DEAD in tetrahydofuran (15 ml) was stirred for 20 hours at room temperature. The mixture was diluted with ether and the solution was washed with saturated aqueous sodium hydrogen carbonate, water, and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue was purified by silicagel column chromatography (ethyl acetate: n-hexane=1:1 ) to give 680 mg (83.3%) of (+)-5-[[(2R, 4S)-4-benzoyloxy-1-(4-methoxyphenethyl)pyrrolidin-2-yl]methyl]-5,11-dihydrodibenzo[b,e][1,4]oxazepine as pale yellow amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436922B1
Source datasetuspto-grants-2002_08
ORD IDord-b2b483d1633744a68dee0138c3b5b065
Source noteuspto-grants-2002_08