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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19790Generated: October 27, 2026

1-Bromo-3-chloro-5-cyclopropylbenzene → (4-Tert-butylbenzyl)-[2-(3-chloro-5-cyclopropylphenyl)-ethyl]-amine

https://huagongshe.com/reaction/19790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloro-5-cyclopropylbenzeneHCID 66520960—
Reactant3-(4-Tert-butylbenzyl)-[1,2,3]oxathiazolidine 2,2-dioxideHCID 86613991—
Product(4-Tert-butylbenzyl)-[2-(3-chloro-5-cyclopropylphenyl)-ethyl]-amineHCID 6856271163.8%

Reaction Steps

The title compound was synthesized in analogy to example S6-C using 1-bromo-3-chloro-5-cyclopropylbenzene (96 mg, 0.71 mmol) and 3-(4-tert-butylbenzyl)-[1,2,3]oxathiazolidine 2,2-dioxide (36 mg, 0.89 mmol). The residue was purified by flash column chromatography to give the desired product (155 mg, 39%) as a colorless oil. MS (ISP) 342.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745477B2
Source datasetuspto-grants-2010_06
ORD IDord-425dc250e5a54e08a1319a363034105e
Source noteuspto-grants-2010_06