Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656274Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 57262708, compound

https://huagongshe.com/reaction/1656274

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131718222HCID 131718222—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 57262708HCID 5726270872.2%

Reaction Steps

To a solution of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(1-t-butyldimethylsilyloxyethylindol-5-yl)oxy-3"-methoxycyclohexyl)-1'-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone (0.38 gm) in CH2Cl2 (10 ml) at room temperature was added a solution of para-toluene sulfonic acid (0.05 gm) in CH3OH (10 ml). The reaction mixture was stirred for 3 hours until TLC (silica, 2:1, hexanes:ethyl acetate) verified that reaction was complete. The reaction mixture was poured into saturated NaHCO3 and extracted twice with CH2Cl2. The combined organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by chromatography (silica, 2:1 hexanes:ethyl acetate) to provide the title compound 0.245 gm. MASS (FAB)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252732
Source datasetuspto-grants-1993_10
ORD IDord-40cbb9f5f7f84eb2a96e52b02c9f01b8
Source noteuspto-grants-1993_10