HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thymol → Bis(2-isopropyl-5-methylphenyl) chlorothiophosphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thymol | HCID 6989 | — |
| Reactant | Thiophosphoryl chloride | HCID 19883 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | Bis(2-isopropyl-5-methylphenyl) chlorothiophosphate | HCID 19690221 | 63% |
Reaction Steps
2-isopropyl-5-methylphenol was reacted with sodium hydride and thiophosphoryl chloride using the procedure of Example 21 to form bis(2-isopropyl-5-methylphenyl) chlorothiophosphate (31PNMR, singlet, 57 ppm). This compound was reacted with diphenylphosphonothioic amide by the General Method C(ii) (THF) yielding the compound of Formula I in which R1 =R2 =phenyl and R3 =R4 =2-isopropyl-5-methylphenoxy. Yield 63%; titration purity, 90%, MW593; 31PNMR, quartet 53 ppm. Test 2 (Table 2) showed that the product is a very strong extractant for zinc; however on long standing it crystallised from ESCAID solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728853 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-6780bd14b0b34526b70c2eaf4a175924 |
| Source note | uspto-grants-1998_03 |