HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Diisopropyl-(3-pentynyloxy)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Pentyn-1-ol | HCID 66295 | — |
| Reactant | Chlorodi(isopropyl)silane | HCID 2758383 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Diisopropyl-(3-pentynyloxy)silane | HCID 59925975 | — |
Reaction Steps
To a cold (0° C.) solution of 3-pentynol (5.880g, 70.0 mmol, 1.0 equiv), 4-dimethylaminopyridine (DMAP) (840 mg, 7.00 mmol, 0.10 equiv), and triethylamine (TEA) (9.80 ml, 71.0 mmol, 1.01 equiv) in 100 mL of dry hexane was added dropwise chlorodiisopropylsilane (11.0 g, 71.0 mmol, 1.01 equiv) over 20 minutes. The resulting white suspension was allowed to warm to room temperature and was stirred overnight. The reaction mixture was filtered through a short silica pad (10 g) and the solvent was then evaporated in vacuo to give a colorless liquid. Fractional distillation of this liquid afforded 11.2 g (81%) of A-7 as a colorless liquid. An analytical sample (0.48 g) was obtained by redistillation of a 0.50 g sample by Kugelrohr distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867323B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-eba02fa127c64d0dac4a65085aeffd8c |
| Source note | uspto-grants-2005_03 |