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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022708Generated: October 29, 2026

Water → tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-butyl (6R,7R)-6-[2-amino-2-(hydroxyimino)ethyl]-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 86663870—
SolventTolueneHCID 1140—
Producttert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-[(5-methyl-1,2,4-oxadiazol-3-yl)methyl]-1,4-oxazepane-4-carboxylateHCID 6697505444.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of tert-butyl (6R,7R)-6-[2-amino-2-(hydroxyimino)ethyl]-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (388 mg, 0.93 mmol) in toluene (4 mL) were added potassium tert-butoxide (208 mg, 1.86 mmol) and ethyl acetate (1 mL, 0.93 mmol). The reaction mixture was stirred at 100° C. overnight. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (183.4 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-8a01925d028f401f8bd52d60c27b241f
Source noteuspto-grants-2014_05