HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880595Generated: October 30, 2026
Methyl 4-(bromomethyl)benzoate → HCID 59756929, compound
https://huagongshe.com/reaction/1880595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 69307037 | HCID 69307037 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59756929 | HCID 59756929 | — |
Reaction Steps
Sodium t-butoxide (67 mg, 0.70 mmol) was added all at once to a THF solution (4 mL) containing the intermediate from Step B (250 mg, 0.668 mmol) stirred at −78° C. After 2 minutes 4-bromomethyl-benzoic acid methyl ester (161 mg, 0.70 mmol) was added all at once. The reaction solution was allowed to warm to room temperature. After stirring for 1 hour the reaction solution was partitioned between aqueous 1N HCl and ethyl acetate. The organic phase was washed with brine and dried over MgSO4. The solution was filtered, concentrated and the residue purified by silica gel chromatography using a hexanes/ethyl acetate gradient to give the title compound. 1H NMR (500 MHz, CDCl3): δ 7.92-7.90 (m, 2H); 7.79-7.75 (m, 1H); 7.51-7.49 (m, 2H); 7.47-7.32 (m, 4H); 7.30-7.27 (m, 2H); 7.24-7.19 (m, 3H); 7.17-7.15 (m, 1H); 7.05 (dd, J=8.3, 11.3 Hz, 1H); 4.88 (t, J=7.4 Hz, 1H); 3.91 (s, 3H); 3.68 (dd, J=7.1, 13.7 Hz, 1H); 3.17 (dd, J=7.6, 13.7 Hz, 1H). LCMS1 4.40 min. (M+H)− 523
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08318760B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-485f1ac8a648418798d317d35d79adce |
|---|
| Source note | uspto-grants-2012_11 |
|---|