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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086105Generated: October 26, 2026

Bromide ion → 2,2'-Thiodipyridine

https://huagongshe.com/reaction/1086105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178418616HCID 178418616—
SolventDimethylformamideHCID 6228—
SolventN-methyl-N-(propan-2-yl)formamideHCID 14529853—
Product2,2'-ThiodipyridineHCID 521114—

Reaction Steps

1.11 g of 2-mercaptopyridine and 0.48 g of 50% sodium hydride were dissolved in 25 ml of dimethyl formamide, and the mixture was stirred at room temperature for 1 hour. A solution of 6.5 g of polyprenyl bromide of general formula (II) in which n is 15 and A2 is Br in 5 ml of dimethyl N,N-dimethylformamide was added dropwise. After the addition, the mixture was stirred overnight at room temperature. The reaction mixture was poured into about 50 ml of water, and extracted with diethyl ether. Then, the diethyl ether layer was washed with water and dried over anhydrous magnesium sulfate. The ether was distilled off to give a yellow liquid. The liquid was purified by silica gel column chromatography using hexane/ethyl acetate as an eluent to give 3.9 g of a slightly yellow liquid. The NMR analysis of this liquid showed that the signal (doublet, δ=3.91) assigned to --CH2Br of the starting polyprenyl bromide disappeared, and a signal (doublet, δ=3.78) assigned to --CH2S and a signal (multiplet, δ=6.75-8.35) assigned to --S--C5H4N newly appeared. The FD-MASS analysis of this liquid gave m/e=1335.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05012018
Source datasetuspto-grants-1991_04
ORD IDord-ae42f2a4687246f7a2e64c038dc9626c
Source noteuspto-grants-1991_04