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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488742Generated: November 4, 2026

Ethanol → HCID 22906421, compound

https://huagongshe.com/reaction/1488742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4'-ChloropropiophenoneHCID 22697—
ReactantEthyl orthoformateHCID 31214—
ProductHCID 22906421HCID 2290642188%

Reaction Steps

A solution of 15.0 g of p-chloropropiophenone and 7.8 mL of dry EtOH was treated with 22.0 mL of triethyl orthoformate. Gaseous HCl was bubbled through the solution until saturation and the reaction mixture heated to reflux overnight. An additional 14.8 mL of triethyl orthoformate was added and the reaction mixture allowed to cool to room temperature. The cooled mixture was washed with 10 % Na2CO3, extracted with diethyl ether and concd in vacuo to afford 19.0 g (88%) of a crude orange/yellow oil. The oil was distilled and a fraction collected (75°-96° C., 100 mtorr) which contained 13.4 g of 1-chloro-4-(1,1-diethoxypropyl)benzene: μ (23,D) 1.5612; 1HNMR (CDCl3) a 0.56 (t, 3H, 7.5 Hz), 1.19 (t, 6H, 7.0 Hz), 1.89 (q, 2H, 7.5 Hz), 3.36 (m, 4H), 7.28 (d, 2H, 8.5 Hz), 7.42 (d, 2H, 8.5 Hz). Anal. Calcd for C13H19O2Cl: C, 64.32;H, 7.89. Found: C, 64.09; H, 7.81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05675017
Source datasetuspto-grants-1997_10
ORD IDord-67be2f6586e04bb3890698400278949b
Source noteuspto-grants-1997_10