HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-(3-Methylbutoxy)-2-propylthiophenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | S-5-(3-methylbutoxy)-2-propylphenyl N,N-dimethylthiocarbamate | HCID 21545974 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | 5-(3-Methylbutoxy)-2-propylthiophenol | HCID 21545985 | — |
Reaction Steps
A solution of 136.1 parts of S-5-(3-methylbutoxy)-2-propylphenyl N,N-dimethylthiocarbamate and 280 parts of potassium hydroxide in 1000 parts of digol was stirred under nitrogen at 120° - 130° for 9 hours, after which no dimethylamine could be detected in the effluent nitrogen. The mixture was cooled, poured into 8000 parts of water and the resulting solution was acidified to pH 1 with hydrochloric acid. The mixture was extracted with ether and the latter was washed with water, dried over magnesium sulphate, filtered and evaporated to dryness to give 95.7 g of the desired product 5-(3-methylbutoxy)-2-propylthiophenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03952013 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-b1f54d07f00b402ab11bb08dbc9756b0 |
| Source note | uspto-grants-1976_04 |