HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10546047, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2-(5-Bromo-1H-indol-1-yl)ethanol | HCID 10657650 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10546047 | HCID 10546047 | — |
Reaction Steps
A solution of 1(2-hydroxyethyl)-5-bromoindole (6 gm, 0.025 mol), t-butyldimethylsilyl chloride (4.5 gm, 0.03 mol) and triethylamine (4.2 ml, 0.03 mol) in CH2Cl2 (60 ml) was stirred for 12 hours at room temperature. The reaction mixture was then washed twice with H2O, dried over Na2SO4, filtered and concentrated in vacuo to provide the title compound as a yellow oil. 1H NMR was consistent with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05352783 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-1d1c0232189d4b10932585f32367bcba |
| Source note | uspto-grants-1994_10 |