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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706939Generated: October 30, 2026

Benzyl Bromide → HCID 10317544, compound

https://huagongshe.com/reaction/1706939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 10108207HCID 10108207—
ProductHCID 10317544HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209527
Source datasetuspto-grants-1980_06
ORD IDord-e0baa28a48584e8a87b3a7f3705dee67
Source noteuspto-grants-1980_06