HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Dodecyloxy-2-decyloxy-1-triphenylmethoxypropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromodecane | HCID 8173 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Dodecyloxy-1-triphenylmethoxy-2-propanol | HCID 15926804 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Dodecyloxy-2-decyloxy-1-triphenylmethoxypropane | HCID 21873196 | 52% |
Reaction Steps
3-Dodecyloxy-1-triphenylmethoxy-2-propanol (13.5 g, 0.027 mol) was added dropwise to an ice-cooled suspension of sodium hydride (80%, 1.6 g, 0.054 mol) in 150 mL of tetrahydrofuran under nitrogen. After stirring for 2 h at room temperature, heat was applied (55° C.). 1-Bromodecane (6 g, 0.027 mol) was added dropwise, and heating continued for 6 h. After cooling for 3 h, water was added slowly. Diethyl ether (2×100 mL) was added, and the solution washed with 15% sodium thiosulfite, water, and brine. After drying over sodium sulfate, the ether was removed, and the residue chromatographed with a gradient of hexanes:ethyl acetate (100:0 to 20:1) to give 9 g (52%) of a clear liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05770584 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-5ac25e0337184591bee0d3084740f077 |
| Source note | uspto-grants-1998_06 |