HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,3-Bis(phenylsulfanyl)propan-2-yl prop-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Acrylate | HCID 25188 | — |
| Reactant | HCID 54113391 | HCID 54113391 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,3-Bis(phenylsulfanyl)propan-2-yl prop-2-enoate | HCID 23070534 | — |
| Product | HCID 53839207 | HCID 53839207 | — |
Reaction Steps
1,3-bis(phenylthio)-2-propyl acrylate was prepared by using benzenethiol in place of dodecanethiol in the procedures described in Steps (1) and (2) of Example 1. A solution of 15 grams of the acrylate, 5 grams of benzenethiol, and 1 milliliter of "Triton B" in 75 milliliters of ethanol was heated under reflux for 51/2 hours. The reaction mixture was allowed to cool and was then poured into water. The oil which precipitated was separated by extraction with toluene. The toluene solution was stripped of solvent on a rotary evaporator leaving 19.8 grams of 1,3-bis-(phenylthio)-2-propyl 3-(phenylthio)propionate which was identified by means of its NMR spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370434 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-9a6020fbb96549ffa8051e4fe1485510 |
| Source note | uspto-grants-1983_01 |