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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641506Generated: November 1, 2026

Diethyl Ether → HCID 57425853, compound

https://huagongshe.com/reaction/1641506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 57425854HCID 57425854—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductHCID 57425853HCID 57425853—

Reaction Conditions

Temperature60 °C

Reaction Steps

Zinc dust was added to a solution of 3-(benzyloxyethyl)-2,2-dichlorocyclobutanone in glacial acetic acid at room temperature. The reactants were heated at 60° C. for 1 hr, after which time dry diethyl ether was added to the cooled products, which were then filtered. The residue was washed with diethyl ether and the combined filtrate and washings were concentrated under reduced pressure. The residue was dissolved in CH2Cl2, which was washed with saturated NaHCO3 twice and water once. The organic phase was dried over MgSO4 and the solvent was evaporated to give an oily product, which was purified by silica gel flash chromatography (Hexane: EtOAc=6:1). 1H NMR (CDCl3, 400 MHz): δ 1.85-1.90 (q, J=6.0, 2H), 2.45-2.56 (m, 1H), 2.66-2.74 (m, 2H), 3.07-3.15 (m, 2H), 3.48-3.51 (t, J=6.0, 2H), 4.48 (s, 2H), 7.24-7.35 (m, 5H). 13C NMR (CDCl3, 100 MHz): δ 21.29, 36.02, 52.56, 68.85, 72.99, 127.56, 127.62, 128.40, 138.33, 208.25. Rf=0.45 (Hexane: EtOAc=3:1). IR (neat) νmax 3054, 2927, 2856, 1779, 1266, 737, 704.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114994B2
Source datasetuspto-grants-2012_02
ORD IDord-8d3bfda43e004d3c857bf493e0e2eed1
Source noteuspto-grants-2012_02