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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865561Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 86749609, compound

https://huagongshe.com/reaction/865561

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 57132476HCID 57132476—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 86749609HCID 8674960967.6%

Reaction Steps

To a stirred solution of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(6"'-tert-butyldimethylsilyloxynaphth-2-yloxy)-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 (73 mg, 0.07 mmol) in CH2Cl2 (2 mL) was added a solution of p-toluenesulfonic acid in methanol (2 mL, 10% solution). The flask was capped and the mixture stirred 4 hours. The reaction was quenched with saturated aqueous NaHCO3 and extracted 4× with CH2Cl2. The organic extracts were combined and dried over anhydrous Na2SO4. The mixture was filtered and concentrated in vacuo. The product was isolated by preparative TLC on silica gel (eluted with 2:1 hexanes/acetone) to afford 44.2 mg of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(6"'-hydroxynaphth-2-yloxy)-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 (Rf =0.23). (1H NMR and mass spectral analysis were consistent with the desired structure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05565560
Source datasetuspto-grants-1996_10
ORD IDord-e2f4409914ab4ccd990dc88da0705450
Source noteuspto-grants-1996_10