HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobenzyl bromide → HCID 53889498, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | HCID 10021814 | HCID 10021814 | — |
| Product | HCID 53889498 | HCID 53889498 | 60% |
Reaction Steps
The 4-[(3-hydroxy-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)carbonyl]benzoic acid methyl ester (from Example 7) was alkylated with 4-bromobenzylbromide as described for Example 60 to give 4-[(3-(4-bromobenzyloxy)-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)carbonyl]benzoic acid methyl ester (60%): 1H NMR (400 MHz, CDCl3) δ 8.03 (1/2ABq, 2H, J=8.4 Hz, ArH), 7.80 (1/2ABq, 2H, J=8.4 Hz, ArH), 7.46 (s, 1H, ArH), 7.29 (1/2ABq, 2H, J=8.4 Hz, ArH), 6.87 (s, 1H, ArH), 6.81 (1/2ABq, 2H, J=8.4 Hz, ArH), 4.87 (s, 2H, OCH2), 3.97 (s, 3H, OCH3), 1.70 (m, 4H, 2CH2), 1.30 (s, 6H, 2CH3), 1.27 (s, 6H, 2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06545049B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-bfd7b91995e5454ebd0107f77370b52c |
| Source note | uspto-grants-2003_04 |