HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601498Generated: October 30, 2026
Ethyl diazoacetate → HCID 12425355, compound
https://huagongshe.com/reaction/601498
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 3-Oxopropyl acetate | HCID 87700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12425355 | HCID 12425355 | 31.2% |
Reaction Steps
Charge a round-bottom flask with tin(II) chloride (16.6 g, 0.088 mol), purge with nitrogen, and add dichloroethane (300 mL) by cannula. Add ethyl diazoacetate (92 mL, 0.88 mol) by cannula and stir 10 min. Add a solution of acetic acid 3-oxo-propyl ester (0.44 mol) in CH2Cl2 (600 mL) slowly by cannula over 1 h, then stir the reaction in a 50° C. oil bath for 3 h. Concentrate under vacuum, add saturated aqueous NaHCO3 and remove the organic phase. Extract the aqueous portion with EtOAc (2×). Wash the combined organic portions with brine, dry over MgSO4, filter through Celite®, and concentrate under vacuum. Purify by flash chromatography on silica gel, eluting with a gradient of EtOAc/hexane 8%-25% to give the title compound (27.8 g, 31%), exact mass 202.08, mass spectrum (ES) 225.1 (M+Na). 1H NMR (CDCl3): δ 4.34 (t, J=6.1 Hz, 2H), 4.20 (q, J=7.1 Hz, 2H), 3.46 (s, 2H), 2.89 (t, J=6.1 Hz, 2H), 2.03 (s, 3H), 1.28 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902356B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-70aac20204094b1cab8e841ca2346fa0 |
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| Source note | uspto-grants-2011_03 |
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