HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948660Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 59450529, compound
https://huagongshe.com/reaction/1948660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | HCID 59450539 | HCID 59450539 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59450529 | HCID 59450529 | — |
Reaction Steps
TsOH (850 mg, 9.449 mmol) was added to a stirred mixture of 1-hydroxy-2,3-dihydro-1H-inden-5-yl benzoate (120 g, 472.441 mmol) and MgSO4 (113.4 g, 944.882 mmol) in toluene at rt under nitrogen, and the reaction mixture was stirred at 90-100° C. overnight. The solid was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (PE) to give the title compound. 1H-NMR (400 MHz, CDCl3): δ 8.22-8.24 (m, 2H), 7.62-7.66 (m, 1H), 7.50-7.54 (m, 2H), 7.42 (d, J=8.1 Hz, 1H), 7.34 (d, J=1.2 Hz, 1H), 7.12 (dd, J=8.1 Hz, J=2.0 Hz, 1H), 6.88-6.90 (m, 1H), 6.57-6.59 (m, 1H), 3.44 (s, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399507B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-6e55e09f7072496785f63414bf45b088 |
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| Source note | uspto-grants-2013_03 |
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