HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 86601638, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 59255008 | HCID 59255008 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86601638 | HCID 86601638 | 84.3% |
Reaction Steps
To a solution of compound 38 (50 mg, 0.13 mmol) and TEA (74 μL, 0.53 mmol) in dry CH2Cl2 (2 mL) was slowly added benzyl bromide (32 μL, 0.27 mmol) at 0° C. and stirred for 5 h. Solvent was removed under reduced pressure. The crude product was purified on a silica gel column chromatography (90:5 CH2Cl2/MeOH) to give a colorless oil (51 mg, 84% yield): 1H NMR (300 MHz, CDCl3) 1.05˜1.72 (m, 9H); 1.74˜1.85 (m, 1H); 1.90˜1.94 (m, 1H); 1.96˜2.05 (m, 1H); 2.31 (d, J=13.0 Hz, 1H); 2.48˜2.52 (m, 1H); 2.88˜2.91 (m, 1H); 3.12 (d, J=18.6 Hz, 1H); 3.67 (dd, J=13.4 Hz, 2H); 7.03˜7.38 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691874B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-524ea5f7354842959c67d8ab58e5a7c9 |
| Source note | uspto-grants-2010_04 |