HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271269Generated: November 1, 2026
Water → 5-(Benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthalene
https://huagongshe.com/reaction/1271269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(Benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthalene | HCID 22932021 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthalene | HCID 22932029 | 54.5% |
Reaction Steps
Under an argon atmosphere, to a solution of 1.82 g of 5-(benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthalene and 0.55 g of 4-(dimethylamino)pyridine in 30 ml of dichloromethane, 1.43 g of p-toluenesulfonyl chloride was added. After 1.2 ml of triethylamine was added dropwise, the mixture was stirred at room temperature for 1.5 hours. The reaction solution was poured into iced water and then extracted with diethyl ether. The extract was washed in turn with 5% hydrochloric acid, water and an aqueous saturated sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1.06 g of the desired compound as a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07205302B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-86fa57b7215a4f6eb1838bf422b7b0c7 |
|---|
| Source note | uspto-grants-2007_04 |
|---|