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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902382Generated: November 1, 2026

Ethanol → 1,3-Bis(phenylsulfanyl)propan-2-yl prop-2-enoate

https://huagongshe.com/reaction/1902382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThiophenolHCID 7969—
ReactantAcrylateHCID 25188—
ReactantHCID 54113391HCID 54113391—
SolventWaterHCID 962—
Product1,3-Bis(phenylsulfanyl)propan-2-yl prop-2-enoateHCID 23070534—
ProductHCID 53839207HCID 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 millilters 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04362887
Source datasetuspto-grants-1982_12
ORD IDord-3d4e6948e56442d3af371f5a7e67cfad
Source noteuspto-grants-1982_12