HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 6,7-Dimethoxynaphthalene-2-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 23721231 | HCID 23721231 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6,7-Dimethoxynaphthalene-2-sulfonyl chloride | HCID 14457754 | — |
Reaction Steps
To a stirred suspension of 50 g of finely divided sodium 6,7-dimethoxy-2-naphthalenesulfonate in 100 ml of dimethylformamide was added dropwise 62.2 ml of thionyl chloride at room temperature. After 30 minutes, the reaction mixture was poured into 1 l of ice water, and the precipitate filtered and then dissolved into 250 ml of benzene. The benzene solution was repeatedly washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated to dryness in vacuo, and the residue was recrystallized from benzene-n-hexane (1 : 1) to give 32 g of 6,7-dimethoxy-2-naphthalenesulfonyl chloride, M.P. 127.5°-129.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073913 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-3b1fc6835a7941f4a8fefc6ba992a02e |
| Source note | uspto-grants-1978_02 |