HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 21506015, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 21506098 | HCID 21506098 | — |
| Reactant | HCID 21506116 | HCID 21506116 | — |
| Product | HCID 21506015 | HCID 21506015 | — |
Reaction Steps
By replacing, in Example 52 A, 3-amino-4-anilino-5-sulphamyl-benzoic acid (2 g) by 3-amino-4-anilino-5-phenylsulphamyl-benzoic acid (4.4 g) and increasing the amount of benzyl bromide to 3.9 g, ethyl-4-anilino-3-benzylamino-5-phenylsulphamyl-benzoate was obtained with a melting point of 166°-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985777 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-de36ccdea9c544978a9e0c974e19e093 |
| Source note | uspto-grants-1976_10 |