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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169320Generated: November 3, 2026

1,1-Dichloroethane → [2-(Tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopentylamine

https://huagongshe.com/reaction/2169320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DichloroethaneHCID 6365—
ReactantCyclopropylamineHCID 69828—
Reactant2-((Tert-butyldimethylsilyl)oxy)acetaldehydeHCID 4187788—
ReactantSodium borohydrideHCID 4311764—
CatalystAcetic AcidHCID 176—
Product[2-(Tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopentylamineHCID 8672595937.48%

Reaction Steps

To a stirred solution of cyclopropylamine (1 g, 13.15 mmol) in dichlorethane (20 mL) were added 2-(tert-butyl-dimethylsilanyloxy)acetaldehyde (2.3 mg, 2.30 mmol) and acetic acid (0.08 mL, 0.29 mmol) at 0° C. Stirring was continued for 24 h at room temperature and NaBH4 (995 mg, 26.29 mmol) was added portion-wise at 0° C. The reaction mixture was further stirred for 2 h at room temperature, quenched with water and extracted with dichloromethane (3×30 mL). The organic part was dried and concentrated to yield a crude product which was purified by Combi-Flash column (eluted at 10-20% ethyl acetate in hexane) to get [2-(tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopentylamine (8e) (1.2 g, 37.48%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-f47caab5cbfd4c2097a8cbdf4a246e4e
Source noteuspto-grants-2015_06