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 produced in the same manner as in Preparation Example 1, except that the mixed diaminotoluene was used in place of the first diaminotoluene. It was confirmed that tolylene dicarbamate was obtained at a yield of 95 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748654B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-bd7fbbf4f6444cb98fae4e1093f04e03 |
| Source note | uspto-grants-2014_06 |