HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37782Generated: October 25, 2026
Propyl p-toluenesulfonate → p-Toluenesulfonic acid
https://huagongshe.com/reaction/37782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propyl p-toluenesulfonate | HCID 69035 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | 50% |
Reaction Steps
A 72 liter unjacketed reactor was charged with 1.84 kg (10.87 mol) of R(+)-2,6 diamino-4,5,6,7-tetrahydro-benzothiazole (R(+) diamine), followed by 14.7 L of dimethyl formamide (DMF). Under continuous stirring, the mixture was heated to a temperature of between 65° C. and 68° C. A solution of 2926 grams propyl tosylate and 1761 grams diisopropylethyleamine in 3.455 L DMF was added slowly over a period of 2 hours. The reaction was continued at 67° C. for an additional 4 hours, after which the solution was gradually cooled to room temperature (18° C. to 22° C.) and stirred for an additional 15 hours. The solution was diluted with 14.72 L of MTBE over a time period of 30 minutes, and stirred for an additional 1 hour. The precipitated material was collected by filtration and washed with 7.32 L, MTBE, followed by 3 washes of 3.68 L each of ethanol, and a wash with 9.2 L heptane. The washed precipitated cake was dried under high vacuum at 30° C. to 35° C. The final weight of the dried product was 2090 grams, representing a 50% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08524695B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-e785ea6338194dd69e22ecc6c663d32e |
|---|
| Source note | uspto-grants-2013_09 |
|---|