HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 53950865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 54567419 | HCID 54567419 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53950865 | HCID 53950865 | 103.3% |
Reaction Steps
Under ice-cooling, to a tetrahydrofuran solution of (R)-1-t-butyldimethylsiloxy-2-methoxymethoxy-3-(2-methoxyphenyl)propane (2.2 g) was added a solution of n tetrabutylammoniumfluoride (1 mol/l, 6.46 ml) in tetrahydrofuranand stirred for 2 hours successively. After tetrahydrofuran wasevaporated in vacuo, water was added, extracted with ethyl acetate,and dried over magnesium sulfate. The solvent was evaporated invacuo, the gained crude product was purified by silica gel columnchromatography, and eluted with a mixed solvent of hexane andethyl acetate (1:1, v/v). The fractions containing the desiredproduct were combined and evaporated in vacuo to obtain (R)-2-methoxymethoxy-3-(2-methoxyphenyl)-1-propanol(1.51 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05514773 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-6621b6ece03348978c4fb598a9126fd4 |
| Source note | uspto-grants-1996_05 |