HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 7-(1-Adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 3-(Adamantan-1-yl)-6-bromonaphthalen-2-ol | HCID 14549072 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-(1-Adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene | HCID 19694681 | — |
Reaction Steps
11.9 g (33.3 mmol) of 7-(1-adamantyl)-6-hydroxy-2-bromonaphthalene, 120 ml of DMF, 5.1 ml (36.6 mmol) of triethylamine and 203 mg of 4-dimethylaminopyridine were introduced successively into a three-necked flask. A solution of 5.52 g (36.6 mmol) of tert-butyldimethylsilyl chloride was added dropwise and the mixture was stirred at room temperature for 12 hours. The reaction medium was poured into water, extracted with ethyl ether, the organic phase decanted, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a silica column eluted with heptane; 12 g (76%) of 7-(1-adamantyl)-6-tert-butyldimethylsilyloxy-2-bromonaphthalene of melting point 120°-121° C. were recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723499 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-a18ffbdb8f6b474a86827045ded0ce46 |
| Source note | uspto-grants-1998_03 |