HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Diaminotoluene → HCID 86712415, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Diaminotoluene | HCID 17593 | — |
| Reactant | HCID 14008947 | HCID 14008947 | — |
| Product | HCID 86712415 | HCID 86712415 | — |
| Product | HCID 86712416 | HCID 86712416 | — |
Reaction Steps
Tolylene dicarbamate was obtained in the same manner as in Example 1, except that the reaction time in the carbamate-forming reaction was set to 10 hours and that 8 g of the decomposed diaminotoluene (second diaminotoluene) obtained in Preparation Example 2 was blended with 100 g of the first diaminotoluene in the mixing step. It was confirmed that tolylene dicarbamate was obtained at a yield of 98 mol % as the total amount of 2,4-bis(butoxycarbonylamino)toluene (2,4-tolylene dicarbamate) and 2,6-bis(butoxycarbonylamino)toluene (2,6-tolylene dicarbamate). The isomer ratio of the mixed diaminotoluene was 2,4-diaminotoluene/2,6-diaminotoluene=81.1/18.9 (molar ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748654B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-734cf274ce8642c98829cdbbffece3a9 |
| Source note | uspto-grants-2014_06 |