HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Hydroxy-3-bromo-4-methoxy-(1,1-dimethylethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehyde | HCID 19861827 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Hydroxy-3-bromo-4-methoxy-(1,1-dimethylethyl)benzaldehyde | HCID 19861815 | 69.3% |
Reaction Steps
A solution of 2.56 g (12.3 mmol) of 2-hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehyde and 2.19 g (12.3 mmol) of N-bromosuccinimide in 20 ml of methylene chloride was stirred for 6 hours. Water (50 ml) was added. The organic phase was dried and evaporated. The residue was chromatographed on silica gel (36 g) using 2:98 (v/v) ether/hexane as eluent. There was obtained 2.45 g (8.53 mmol, 69%) of 2-hydroxy-3-bromo-4-methoxy-(1,1-dimethylethyl)benzaldehyde as white crystals after crystallization from cyclohexane; mp 123°-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04910202 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-5402824a46e04fb58d264b6117d78d30 |
| Source note | uspto-grants-1990_03 |