HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 59161057, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59161040 | HCID 59161040 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59161057 | HCID 59161057 | — |
Reaction Steps
The crude product from Example 2A is dissolved in 20 ml of dichloromethane, and 0.83 ml (5.93 mmol) of triethylamine and 1.54 ml (5.93 mmol) of tert-butyldiphenylchlorosilane are added. After addition of 24.2 mg (0.20 mmol) of 4-N,N-dimethylaminopyridine the mixture is stirred at RT for 20 h. In each case 10 ml of ethyl acetate and of saturated aqueous sodium bicarbonate solution are then added. The phases are separated, and the combined organic phases are then dried over magnesium sulfate. The solvent is removed on a rotary evaporator and the residue is purified chromatographically on silica gel 60 (mobile phase: gradient cyclohexane/ethyl acetate 100:1→20:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304412B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-8d374be8e03f4d31a6b5a2fb71ba5e75 |
| Source note | uspto-grants-2012_11 |