HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 10317544, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 10108207 | HCID 10108207 | — |
| Product | HCID 10317544 | HCID 10317544 | — |
Reaction Steps
The procedure described in Example 1 was repeated (using the same molar proportions as before) except that 210 mg. (0.0007 mole) of 5,6-dichloro-2-oxo-1-benzimidazolineacetic acid ethyl ester (prepared according to the procedure described in Preparation A) and 120 mg. (0.0007 mole) of benzyl bromide were reacted to afford crude 3-benzyl-5,6-dichloro-2-oxo-1-benzimidazolineacetic acid ethyl ester, which was used as such in the next reaction step (viz., hydrolysis to the corresponding acid as hereinafter described in Example 24) without any further purification being necessary.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04209527 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-e0baa28a48584e8a87b3a7f3705dee67 |
| Source note | uspto-grants-1980_06 |