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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727233Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 86614069, compound

https://huagongshe.com/reaction/1727233

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 86614067HCID 86614067—
SolventEthylene GlycolHCID 174—
SolventMethanolHCID 887—
ProductHCID 86614069HCID 86614069—

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirred solution of (3aS,4R,6aR,7R,10R,10aR)-7-(2,2-dichloro-1-methylethenyl)-2,2,5,10-tetramethyl-4,6a,7,8, 9,10-hexahydro-3aH-naphtho[1,8a-d][1,3]dioxol-4-yl acetate (Preparation 170, 0.95 g) in ethylene glycol (40 ml) and methanol (10 ml) was added para-toluenesulphonic acid (95 mg). The reaction mixture was heated to 75° C., after 1.5 h the reaction mixture was concentrated in vacuo to remove the methanol. The resultant solution was diluted with diethyl ether (30 ml) and water (30 ml) and the organic layer separated and washed with sodium hydrogen carbonate (3×30 ml). The aqueous layers were back extracted with diethyl ether (2×20 ml) and the combined organic extracts were dried (MgSO4) and concentrated to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-2d302366326f4f54b0eb74a2641d4bad
Source noteuspto-grants-2009_02