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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627022Generated: November 2, 2026

4-Bromo-2-chloroaniline → HCID 58103913, compound

https://huagongshe.com/reaction/1627022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-chloroanilineHCID 610169—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66844375HCID 66844375—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58103913HCID 58103913—

Reaction Conditions

Temperature68 °C

Reaction Steps

To a solution of 4-bromo-2-chloroaniline [C.A.S. 38762-41-3], (1 g, 4.843 mmol) in AcOH (19 ml) and MeOH (10 mL) stirred at room temperature and under nitrogen atmosphere was added dropwise (1-ethoxycyclopropyloxy-trimethylsilane [C.A.S. 27374-25-0] (1.199 ml, 5.57 mmol). The reaction mixture was then refluxed at 67-69° C. for 3 h. The mixture was then concentrated in vacuo to yield intermediate D30′. In another flask, NaBH4 (0.366 g, 9.687 mmol) was suspended in THF (10 mL) and cooled to 5° C. Then, BF3.Et2O complex (1.228 ml, 9.687 mmol) was added dropwise. The resulting reaction mixture was stirred under a N2 atmosphere at 5° C. for 1 h. Then, to this mixture was added a solution of D30′ in THF (5 mL) dropwise at 5-10° C. over 20 min. After stirring at r.t. for 5 h., at reflux temperature for 2 h., and then removing THF by distillation, the mixture was cooled to r.t. and poured into water. The resulting mixture was extracted with Et2O. The organic layer was washed with water and dried (Na2SO4) followed by the removal of the volatiles under vacuo. The crude product thus obtained was purified by column chromatography (silica gel; Heptane/EtOAc 99:1 as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate compound D30 (0.390 g, 32.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785486B2
Source datasetuspto-grants-2014_07
ORD IDord-ee4b10658dc14e548aa20cdf0011cee7
Source noteuspto-grants-2014_07