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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400353Generated: October 31, 2026

(3-Bromo-4-((5-phenylpentyl)amino)phenyl)methanol → 3-Bromo-4-((5-phenylpentyl)amino)benzaldehyde

https://huagongshe.com/reaction/400353

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Bromo-4-((5-phenylpentyl)amino)phenyl)methanolHCID 86687855—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product3-Bromo-4-((5-phenylpentyl)amino)benzaldehydeHCID 86687854—

Reaction Steps

A solution of 5-bromopentylbenzene [14469-83-1](4 g, 17.6 mmol) in HMPA (55 g) was treated with 4-amino-3-bromobenzemethanol [146019-46-7] and dry K2CO3 (4.87 g, 35.2 mmol) for ˜18 h at 120° C. The mixture was cooled to rt, poured onto water (600 mL) and extracted with ethyl acetate (200 mL). The organic phase was washed with water (200 mL), dried over Na2SO4, concentrated, and purified by chromatography (ethyl acetate/hexane) to give (3-bromo-4-((5-phenylpentyl)amino)phenyl)methanol (2.24 g, 37%). A solution of (3-bromo-4-((5-phenylpentyl)amino)phenyl)methanol (8.0 g, 23 mmol) in dichloromethane (160 mL) was treated with silica gel (24 g) and PCC (14.9 g, 69 mmol) at rt for ˜18 h. The mixture was concentrated, and purified by chromatography on silica gel (ethyl acetate-hexane) to give 3-bromo-4-((5-phenylpentyl)amino)benzaldehyde Intermediate-21 (3.5 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741875B2
Source datasetuspto-grants-2014_06
ORD IDord-82544e20936a497e90e496fc7c700a7c
Source noteuspto-grants-2014_06