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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898852Generated: October 30, 2026

Water → HCID 86607498, compound

https://huagongshe.com/reaction/898852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 67525593HCID 67525593—
ReactantHCID 86607499HCID 86607499—
SolventAcetonitrileHCID 6342—
ProductHCID 86607498HCID 86607498—

Reaction Steps

p-Toluenesulfonic acid monohydrate (5.2 g, 27 mmol) was added to a solution of the crude product (5.0 g) of (1R*,2S*)-2-azidomethyl-1-t-butoxycarbonylamino-2-phenyl-cyclopropanecarboxylic acid t-butyl ester, which was made from (1R*,2S*)-1-t-butoxycarbonylamino-2-hydroxymethyl-2-phenyl-cyclopropanecarboxylic acid t-butyl ester obtained in Preparation Example 2-6 by general method step 5-3, in acetonitrile (40 mL). The mixture was stirred at room temperature for 14 hours. After water (16 mL) was added, the mixture was further stirred for 7 hours and separated into layers by adding ethyl acetate (50 mL). The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution (30 mL), water (30 mL) and saturated aqueous sodium chloride solution (50 mL), and dried over sodium sulfate. The residue was filtrated and the solvent was evaporated to give a crude product of the title compound (2.8 g). The obtained product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351825B2
Source datasetuspto-grants-2008_04
ORD IDord-7c43ea6e3b3c4f2d966591aefcad706e
Source noteuspto-grants-2008_04