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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2S,3S)-(-)-3-tert-Butoxycarbonylamino-1,2-epoxy-4-phenylbutane | HCID 9903372 | — |
| Reactant | HCID 178477761 | HCID 178477761 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59570099 | HCID 59570099 | 54.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08299267B2 |
|---|
| Source dataset | uspto-grants-2012_10 |
|---|
| ORD ID | ord-10d1a9508caf4afda6f97ccdaff122d1 |
|---|
| Source note | uspto-grants-2012_10 |
|---|