HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → tert-butyl-2-(N-Boc-3-hydroxy-azetidin-3-yl)-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Oxo-azetidine-1-carboxylic acid tert-butyl ester | HCID 1519404 | — |
| Reactant | HCID 178451183 | HCID 178451183 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl-2-(N-Boc-3-hydroxy-azetidin-3-yl)-acetate | HCID 58520848 | — |
Reaction Steps
To a stirring solution of N-Boc-3-azetidinone (0.45 g, 2.64 mmol) in THF (5 mL) was slowly added a 0.5 M solution of 2-tert-butoxy-2-oxoethyl -zinc chloride in Et2O (10 mL, 5.0 mmol), and the reaction mixture was stirred for 5 h. The reaction was then quenched with sat. aq. NH4Cl (10 mL), and the aqueous layer was separated and extracted with ethyl acetate (2×30 mL). The combined organic layers were washed with 5% aq. NaHCO3 (2×10 mL), brine (15 mL), dried over Na2SO4, filtered and concentrated to dryness to yield tert-butyl-2-(N-Boc-3-hydroxy-azetidin -3-yl)-acetate (MS m/e [M−H]+ calcd 288.2, found 287.7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524675B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-ca40cd7519814254853942a10488ac7e |
| Source note | uspto-grants-2013_09 |