HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 68583816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Prop-2-en-1-yl)-5,6,7,8-tetrahydronaphthalen-1-ol | HCID 68583287 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Product | HCID 68583816 | HCID 68583816 | 88.2% |
Reaction Steps
Treatment of 2-allyl-5,6,7,8-tetrahydronaphthalen-1-ol (18.48 g, 0.098 mol) with potassium carbonate (41.46 g, 0.300 mol), benzyl bromide (18.81 g, 0.110 mol), and tetrabutylammonium iodide (7.39 g, 0.020 mol) generally according to the procedure described for Intermediate 1 afforded 24.05 g (88%) of 2-allyl-5,6,7,8-tetrahydronaphthalen-1-yl benzyl ether as a pale yellow oil. Rf=0.39 (silica, ethyl acetate:hexanes 1:19); Anal. calcd. for C20H22O0.2H2O: C, 85.19; H, 8.01. Found: C, 84.95; H, 7.75.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728155B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-4af40855a52e4385bf6d7111eeefc971 |
| Source note | uspto-grants-2010_06 |