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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478884Generated: October 25, 2026

Triethylamine → 2-((2-Benzoylphenylthio)methyl)butyraldehyde

https://huagongshe.com/reaction/478884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthylacroleinHCID 70203—
Reactant2-MercaptobenzophenoneHCID 3499713—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-((2-Benzoylphenylthio)methyl)butyraldehydeHCID 2232522364%

Reaction Steps

To an ice bath cooled solution of 9.76 g (0.116 mole) of 2-ethylacrolein in 40 mL of dry THF was added 24.6 g (0.116 mole) of 2-mercaptobenzophenone in 40 mL of THF followed by 13 g, (0.128 mole) of triethylamine. The reaction mixture was stirred at room temperature for 3 days, diluted with ether, and was washed successively with dilute HCl, brine, and 1 M potassium carbonate. The ether layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by HPLC (10% EtOAc-hexane) to give 22 g (64%) of 11 in the second fraction. An attempt to further purify this material by kugelrohr distillation at 0.5 torr (160-190° C.) gave a fraction (12.2 g) which contained starting material indicating a reversed reaction during distillation. This material was dissolved in ether (100 mL) and was washed with 50mL of 1 M potassium carbonate three times to give 6.0 g of a syrup which was purified by HPLC (10% EtOAc-hexane) to give 5.6 g of pure 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642268B2
Source datasetuspto-grants-2003_11
ORD IDord-65e628fab7e4417b981e4e8fa649ae8e
Source noteuspto-grants-2003_11