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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734336Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 57020357, compound

https://huagongshe.com/reaction/1734336

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 57193466HCID 57193466—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 57020357HCID 5702035764.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(4'"-tert-butyldimethylsilyloxyphenyloxy)-3"-hydroxycyclohexyl)-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 (41.9 mg) in CH2Cl2 (1.5 mL.) at 0° C. was added a solution of p-toluenesulfonic acid in methanol (1.5 mL. of a 10% w/v solution). The mixture was stirred 3 H at 0° C. and then 3 H at room temperature. The reaction mixture 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) affording 23.9 mg of 17-ethyl-1,14-dihydroxy-12-[2'-(4"-(4'"-hydroxyphenyloxy)-3"-hydroxycyclohexyl)-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. (1H NMR and mass spectral analysis are consistent with the desired structure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532248
Source datasetuspto-grants-1996_07
ORD IDord-64d6051d24924eadabcec9f309c91dbb
Source noteuspto-grants-1996_07