HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591271Generated: October 30, 2026
Benzyl chloroformate → HCID 57219190, compound
https://huagongshe.com/reaction/1591271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86745693 | HCID 86745693 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57219190 | HCID 57219190 | 72.1% |
Reaction Steps
A solution of benzyl chloroformate (485 μL, 3.4 mmols) in methylene chloride (2.5 mL) was added dropwise to a stirred, cooled (ice/H2O bath) solution of (±)-t-butyl 2-[cis-3-amino-4-(2-(2-furyl)ethyl)-2-oxoazetidin-1-yl]acetate (1.0 g, 3.4 mmols) and diisopropylethylamine (592 μL, 3.4 mmols) in methylene chloride (10 mL). Stirring was continued with cooling for 0.5 hr and then for 0.33 hr at ambient temperatures. The solution was sequentially washed with 0.05M (pH 4) ammonium phosphate, H2O, dilute aqueous NaHCO3, and saturated NaCl. The solution was dried (Na2SO4) and concentrated, and the residue was chromatographed on SiO2 (50 g) with hexane-ethyl acetate (2:1). The appropriate fractions were combined and concentrated to leave a viscous oil which was crystallized from diethyl ether-hexane to afford the title compound (1.05 g, 72% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05206360 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-a6f4d9dae4a848b6809fb52b7156d361 |
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| Source note | uspto-grants-1993_04 |
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