Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 67006-35-3 | HCID 11220710 | — |
| Reactant | HCID 74085937 | HCID 74085937 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57157305 | HCID 57157305 | 49% |
Reaction Steps
In a 3 liter reaction vessel were placed 1 liter of distilled water, 1 liter of methanol and 157 g of 1,3-di(2-chloroethylsulfonyl)-2-hydroxypropane. The vessel was heated to 46° C. for the purpose of dissolution. Thereto, a solution of 52 g sodium styrenesulfinate dissolved in a mixture of 100 ml of distilled water and 100 ml of methanol was added dropwise over a period of about 1 hour, and the heating and the stirring were further continued for 5 hours. A crystal deposited was filtered off, washed with methanol, and dried in vacuo. Thus, 55 g of M-6 was obtained. The yield was 49%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04396708 |
|---|
| Source dataset | uspto-grants-1983_08 |
|---|
| ORD ID | ord-605952e14ee140f692aaadbc33fe4bc4 |
|---|
| Source note | uspto-grants-1983_08 |
|---|