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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62764Generated: October 26, 2026

3-Bromopentane → 2-Chloro-1-ethoxy-5-iodo-3-(pentan-3-yloxy)benzene

https://huagongshe.com/reaction/62764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopentaneHCID 15738—
Reactant2-Chloro-3-ethoxy-5-iodophenolHCID 67042212—
Product2-Chloro-1-ethoxy-5-iodo-3-(pentan-3-yloxy)benzeneHCID 6704181279%

Reaction Steps

2-Chloro-1-ethoxy-5-iodo-3-(pentan-3-yloxy)benzene (8) (1.2 g, 79%) was prepared from 2-chloro-3-ethoxy-5-iodophenol (7) (1.1 g, 3.7 mmol) using a procedure essentially the same as in step (i) for AAA-001 except that 3-bromopentane was used instead of cyclopentyl bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-8181d3479b6a417fa4adc534e9103e2d
Source noteuspto-grants-2016_09