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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824636Generated: November 1, 2026

Diethyl Ether → HCID 15398356, compound

https://huagongshe.com/reaction/1824636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 131725737HCID 131725737—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
ProductHCID 15398356HCID 15398356—

Reaction Steps

A sample of 4-ferrocenylbenzyl alcohol 16 (630 mg, 2.15 mmol) was added to a suspension of pyridinium chlorochromate (1.22 g, 3.23 mmol) in CH2Cl2 (5 mL) and the mixture was stirred under argon at rt for 18 h. Then Et2O (20 mL) was added and the mixture was filtered through a pad of Celite. The filtrate was concentrated and chromatographed (silica, CH2Cl2/hexanes, 4:1) affording 306 mg (47.8%). TLC (silica, CH2Cl2), Rf=0.35; mp 122–125° C. (lit.35a121–125° C.); 1H NMR δ 4.07 (s, 5H), 4.46 (A2B2, J=1.5 Hz, 2H), 4.47 (A2B2, J=1.5 Hz, 2H), 7.60,7.78 (AA′BB′, J=8.7 Hz, 4H), 9.97 (s, 1H); 13C NMR δ 67.8, 70.5, 70.6, 70.8, 127.0, 127.7, 130.7, 130.7, 134.7, 192.5; EI-MS obsd 290.0406 (M+), calcd exact mass 290.0394; Anal. Calcd for C17H14FeO: C, 70.37; H, 4.86; Found: C, 70.50; H, 4.81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07042755B1
Source datasetuspto-grants-2006_05
ORD IDord-148819563a144424b5704bc7d86b4d6d
Source noteuspto-grants-2006_05