HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Chloride → 3-Benzyloxy-5-isobutylbenzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Methyl 3-benzyloxy-5-(trifluoromethanesulfonyloxy)benzoate | HCID 18945283 | — |
| Reactant | HCID 178448254 | HCID 178448254 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Benzyloxy-5-isobutylbenzoic acid methyl ester | HCID 58528861 | 68% |
Reaction Steps
To a microwave reaction vial was added 3-benzyloxy-5-trifluoromethanesulfonyloxybenzoic acid methyl ester (70 mg, 0.179 mmol), lithium chloride (23 mg, 0.537 mmol), Pd(PPh3)4 (10 mg, 0.009 mmol) and 3 ml of THF. Isobutylzinc bromide (0.5 M in THF) (0.537 mL, 0.269 mmol) was added and the vial sealed. After heating in microwave reactor at 130° for 5 min the reaction mixture was adsorbed onto silica gel and purified by silica gel chromatography using an ethyl acetate-hexane gradient to afford 36 mg (68%) of 3-benzyloxy-5-isobutylbenzoic acid methyl ester. 1H NMR (300 MHz, DMSO-d6) δ 0.850 (d, 6H, J=6 Hz), 1.78-1.92 (m, 1H), 3.84 (s, 3H), 5.16 (s, 2H), 7.11 (d, 1H, J=2 Hz), 7.33-7.48 (m, 7H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08940927B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-b2464f6e83ef43aa9b5d763b1e907120 |
| Source note | uspto-grants-2015_01 |