HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727233Generated: November 1, 2026
p-Toluenesulfonic acid → HCID 86614069, compound
https://huagongshe.com/reaction/1727233
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 86614067 | HCID 86614067 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86614069 | HCID 86614069 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494992B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-2d302366326f4f54b0eb74a2641d4bad |
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| Source note | uspto-grants-2009_02 |
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