HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Thienylmethyl)amine → HCID 12810653, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Thienylmethyl)amine | HCID 34005 | — |
| Reactant | HCID 12810651 | HCID 12810651 | — |
| Product | HCID 12810653 | HCID 12810653 | 94% |
Reaction Steps
182 g of 2-chloro-4-(N-methylanilino)-5-sulfamoylbenzene sulfonic acid phenyl ester (0.4 mol) are reacted with 0.5 liter of 2-thienylmethyl amine according to Example 1. Working up in the manner described in Example 1 gives 200 g of 2-(thienylmethylamino)-4-(N-methylanilino)-5-sulfamoylbenzene sulfonic acid phenyl ester in chromatographically pure form. Yield: 94% of the theory. The product sinters at a temperature above 90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04341773 |
| Source dataset | uspto-grants-1982_07 |
| ORD ID | ord-1185fbf7dc8a40ac803431e50515b5e3 |
| Source note | uspto-grants-1982_07 |