Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194768Generated: October 26, 2026

1,3,5-Trithiane → 2-{Bis(4-fluorophenyl)hydroxymethyl}-1,3,5-trithiane

https://huagongshe.com/reaction/1194768

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-TrithianeHCID 9264—
Reactant4,4'-DifluorobenzophenoneHCID 9582—
ReactantLithiumHCID 3028194—
SolventTetrahydrofuranHCID 8028—
Product2-{Bis(4-fluorophenyl)hydroxymethyl}-1,3,5-trithianeHCID 1432925883.2%

Reaction Conditions

Temperature-60 °C

Reaction Steps

In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-bytyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.4 g of 4,4'-difluorobenzophenone dissolved in 100 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. After stirring at 0° C. for another 1 hour, the reaction mixture thus obtained was poured into ice water and the resulting mixture was extracted with chloroform. The extract was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The crude product thus obtained was recrystallized from ether-hexane to give 5.58 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816475
Source datasetuspto-grants-1989_03
ORD IDord-2b0b1f81f7bf41a88f7434cf1ae8dfdd
Source noteuspto-grants-1989_03