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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596096Generated: October 31, 2026

2-Bromoaniline → HCID 623433, compound

https://huagongshe.com/reaction/1596096

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoanilineHCID 11992—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23703752HCID 23703752—
CatalystCopperHCID 23978—
SolventTetrahydrofuranHCID 8028—
ProductHCID 623433HCID 62343337%

Reaction Steps

A mixture of 16.0 g (46 mmol) of sodium 3-bromo-2-iodobenzoate [prepared from 15.0 g (46 mmol) of 3-bromo-2-iodobenzoic acid (XX) and 1.1 g (46 mmol) of sodium hydride], 19.5 g (100 mmol) of sodium 2-bromoanilide [prepared from 17.3 g (100 mmol) of 2-bromoaniline (XXI) and 2.4 g (100 mmol) of sodium hydride] and a spatula-tipfull of copper powder in 100 ml of tetrahydrofuran was heated to reflux for 9 h. The solvent was distilled off, the residue extracted with 0.5 M aqueous sodium hydroxide, and the resulting suspension subjected to centrifugation. The centrifugate was acidified with diluted hydrochloric acid, the precipitated solid was filtered off and dried under high vacuum. Fractional sublimation under high vacuum yielded 6.3 g (37% of theory) of 3-bromo-2-(2-bromophenylamino)benzoic acid (XXII) as a yellow powder with a melting point of 181-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06290926B1
Source datasetuspto-grants-2001_09
ORD IDord-6cac769a10054e02b8ac0a17f8385168
Source noteuspto-grants-2001_09