HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → HCID 13313521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (2,2-Dichloro-3,3-dimethylcyclopropyl)methanol | HCID 12604182 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13313521 | HCID 13313521 | 95.9% |
Reaction Steps
A solution of 33.8 g of 2,2-dichloro-3,3-dimethylcyclopropane methanol in 200 ml of pyridine was cooled to 0° C., and 38.2 g of p-toluenesulfonyl chloride was added portionwise. The reaction mixture was left to stand for 12 hours in a refrigerator (0° C.), and then poured into 1 liter of ice water. The crystals precipitated were collected by filtration, washed with water, dried in the air, and washed with hexane to give 62 g of 2,2-dichloro-3,3-dimethylcyclopropylmethyl p-toluenesulfonate, the desired compound shown above. The melting point of the product was 96.5° to 97.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514418 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-a7beeba834054c92a6f8a1a4b53a7d3e |
| Source note | uspto-grants-1985_04 |