Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439397Generated: October 23, 2026

1,3-Dithiolane → Ethyl acetate hexane

https://huagongshe.com/en/reaction/439397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DithiolaneHCID 20970—
Reactant2-AminomethylquinolineHCID 3014378—
ReactantHCID 101658032HCID 101658032—
ProductEthyl acetate hexaneHCID 2122620616%

Reaction Steps

This compound was prepared from 1,3-dithiolane derivative of Z-Leu-Abu-COOEt and 2-aminomethylquinoline by the procedure described in Example 38, and purified by column chromatography using AcOEt/hexane 2:1 (16% yield). Yellow solid, single spot on TLC, Rf =0.27 (AcOEt/hexane 2:1), mp 135°-138° C. 1H NMR (CDCl3) ok, MS (FAB) m/e=519 (M+1). Anal: calcd. for C29H34N4O5, 518; C, 67.16; H, 6.60; N, 10.80. Found, C, 66.89; H, 6.68; N, 10.61.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514694
Source datasetuspto-grants-1996_05
ORD IDord-662cdbc14dcd4809ad99d32ccf3e66e0
Source noteuspto-grants-1996_05