HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 86606707, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 86606705 | HCID 86606705 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86606707 | HCID 86606707 | — |
Reaction Steps
To a 0° C. solution of (E)-ethyl 4-[tris-(1-methylethyl)silyloxy]-3-methylbut-2-enoate (5 g, 17.6 mmol) in dry Et2O was added a solution of lithium aluminum hydride (17.6 mL, 17.6 mmol, 1 M in Et2O). After 30 minutes, the reaction mixture was neutralized by dropwise addition of THF followed by addition of a saturated solution of potassium sodium tartrate. The reaction mixture was stirred overnight and then diluted with Et2O. The organic layer was separated and washed with water, dried over MgSO4 and concentrated in vacuo to afford (E)-3-[tris-(1-methylethyl)silyloxy]but-2-en-1-ol as a colorless oil which was used directly into the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07323604B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-c4dbcafbd1014e71af28becfa0ebb6a2 |
| Source note | uspto-grants-2008_01 |