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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071178Generated: November 1, 2026

(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane → HCID 59570099, compound

https://huagongshe.com/reaction/2071178

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutaneHCID 9903372—
ReactantHCID 178477761HCID 178477761—
SolventDichloromethaneHCID 6344—
ProductHCID 59570099HCID 5957009954.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

(3-(aminomethyl)-5-(dimethylamino)phenoxy)methylium (0.0361 g, 0.2 mmol, 1.2 eq) was dissolved in the minimum amount of anhydrous CH2Cl2 under Ar. tert-butyl (S)-1-((S)-oxiran-2-yl)-2-phenylethylcarbamate (0.0439 g, 0.167 mmol, 1 eq) was added with stirring. Anhydrous CH2Cl2 was added dropwise until all of the epoxide had dissolved. The reaction was heated to 50° C. After heating overnight all of the solvent was gone leaving a solid in the flask. Purification via flash chromatography yielded 0.0405 g, (0.091 mmol, 54% yield) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-10d1a9508caf4afda6f97ccdaff122d1
Source noteuspto-grants-2012_10