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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202685Generated: November 1, 2026

Acetic Acid → 2-(2,6-dichlorophenyl)-N-(spiro[2.5]octan-6-ylmethyl)-2-((triethylsilyl)oxy)ethanamine

https://huagongshe.com/reaction/2202685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSpiro(2.5)octane-6-carbaldehydeHCID 86598198—
Reactant2-(2,6-Dichlorophenyl)-2-((triethylsilyl)oxy)ethanamineHCID 123856251—
SolventDichloromethaneHCID 6344—
Product2-(2,6-dichlorophenyl)-N-(spiro[2.5]octan-6-ylmethyl)-2-((triethylsilyl)oxy)ethanamineHCID 123353182—

Reaction Steps

To a solution of 2-(2,6-dichlorophenyl)-2-((triethylsilyl)oxy)ethanamine (248 mg, 0.774 mmol) in DCM (2581 μl) was added spiro[2.5]octane-6-carbaldehyde (107 mg, 0.774 mmol), AcOH (35.5 μl, 0.619 mmol) and NaBH(OAc)3 (246 mg, 1.161 mmol). The slurry mixture was stirred at room temperature for overnight. The mixture was quenched with 0.5 M NaOH and mixture was stirred at rt for 30 min. Evolution of gas was observed. The layers were separated. The organic layer was dried over Na2SO4 and concentrated. The residue was purified by silica gel column chromatography eluting with a gradient of 0% to 100% EtOAc in hexane to give 2-(2,6-dichlorophenyl)-N-(spiro[2.5]octan-6-ylmethyl)-2-((triethylsilyl)oxy)ethanamine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365522B2
Source datasetuspto-grants-2016_06
ORD IDord-57d7248a90594ea79af9d509b20c6609
Source noteuspto-grants-2016_06