HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dichloroethane → [2-(Tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopentylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 2-((Tert-butyldimethylsilyl)oxy)acetaldehyde | HCID 4187788 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Product | [2-(Tert-butyl-dimethylsilanyloxy)-ethyl]-cyclopentylamine | HCID 86725959 | 37.48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045486B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-f47caab5cbfd4c2097a8cbdf4a246e4e |
| Source note | uspto-grants-2015_06 |