HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335383Generated: October 30, 2026
p-Toluenesulfonic acid → p-Toluenesulfonic acid
https://huagongshe.com/reaction/335383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | Methane | HCID 297 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | 665.7% |
Reaction Steps
A reactor was charged at about 20° C. with the compound of formula (I) form A0 (6.075 kg; 1 eq) and dichloromethane (92 L; 15 V). The mixture was stirred (80 rpm) at 20° C. for 15 minutes. After cooling the mixture to 10° C., paratoluene sulfonic acid (PTSA—2.417 kg; 1 eq) was added portion wise. The mixture was stirred at 80 rpm at 10° C. for 1 hour. Then, MTBE (122 L; 15 V) was added portion wise via a feed vessel. The mixture was heated to 45° C. at least 1 h (checking that the reaction was complete by RX/DSC, if it is necessary, continue the contact). After cooling the mixture to 10° C., the precipitated solids were isolated by filtration and washed with MTBE. The product was dried under vacuum at 40° C. to yield the addition salt of compound of formula (I) with PTSA (8.045 kg; yield=97.3%; purity=99.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08884014B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-886ebd7ddb53416091e12d75df5e5a7f |
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| Source note | uspto-grants-2014_11 |
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