HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-3-(tert-Butyldimethylsilanyloxy)-1-phenylpropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (S)-3-Amino-3-phenylpropan-1-ol hydrochloride | HCID 50998248 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-3-(tert-Butyldimethylsilanyloxy)-1-phenylpropylamine | HCID 68287924 | 97.1% |
Reaction Steps
1.50 g of (S)-3-amino-3-phenylpropan-1-ol hydrochloride were initially charged in 20 ml of dichloromethane and then 2.77 ml of triethylamine and 1.30 g of tert-butyldimethylchlorosilane were added. After stirring at room temperature for 3 hours, the reaction solution was extracted three times with 30 ml of water, dried by means of a phase separator cartridge (Isolute®), concentrated by rotary evaporation and dried under high vacuum. This gave the product (2.06 g) with a molecular weight of 265.5 g/mol (C15H27NOSi); MS (ESI): m/e=266 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710050B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-89e938f558014df4a9264b9ff2e9b417 |
| Source note | uspto-grants-2014_04 |