HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (S)-2-Amino-tert-butyldimethylsilyloxypropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | L-Alaninol | HCID 80307 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-Amino-tert-butyldimethylsilyloxypropane | HCID 21474737 | 80% |
Reaction Steps
A mixture of (S)-(+) 2-amino-1-propanol (1.04 g, 13.85 mmol), tert butyldimethylsilyl chloride (2.09 g, 13.85 mmol) and triethylamine (2 ml, 1.05 eq) was stirred in DCM overnight ca 16 h. The reaction was diluted with DCM, washed with water, satd. NH4Cl, brine, dried and evaporated to an oil. Silica gel purification of the crude using 3% MeOH/CH2Cl2 as eluent provided 2-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-ethylamine (1.76 g, 80%); 1H NMR (300 MHz, CDCl3) 0.0 (s, 6H), 0.82 (s, 9H), 0.99 (d, J=6.5 Hz, 3H), 2.22 (bs, 2H), 2.98 (bs, 1H), 3.30 (dd, J=10 Hz, J=17.0 Hz, 1H), 3.48 (dd, J=10.0 Hz, J=4.3 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357718B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-fae61425203747f380bd0ac483452202 |
| Source note | uspto-grants-2013_01 |