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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603651Generated: November 4, 2026

Sodium hydride → HCID 19605261, compound

https://huagongshe.com/reaction/1603651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(4-Iodobutyl)benzeneHCID 12709818—
ReactantHCID 19605253HCID 19605253—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19605261HCID 1960526114%

Reaction Steps

A solution 4-(benzylthio)azetidin-2-one (1.1 g, 5.5 mmol) in dry THF (10 ml) was added dropwise over 10 minutes to a suspension of NaH (0.13 g, 5.6 mmol) in dry THF (5 ml) at -20° C. under a N2 atmosphere. A solution of 1-iodo-4-phenylbutane (1.4 g, 5.5 mmol) in dry THF (10 ml) was added dropwise over 10 minutes at -55° C. After stirring for 18 hours, the mixture was poured onto ice/water (50 g), filtered through hyflo, the THF evaporated under reduced pressure and the residue taken up in ethyl acetate. The solution was washed with brine (×2), dried (MgSO4), evaporated under reduced pressure to a yellow oil which was purified by flash chromatography on silica gel eluted with 5:1, 3:1 then 1:1 petroleun ether/ethyl acetate to give the product as a yellow oil (0.25 g, 14%). 1H NMR δ (CDCl3) 1.5 (4H, m, 2×CH2), 2.6 (2H, m, CH2Ph), 2.85, 3.2 (each 2H, m, H-3 & NCH2), 3.73 (2H, s, SCH2), 4.54 (1H, m, H-4), 7.2 (10H, m, 2×Ph--H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990102
Source datasetuspto-grants-1999_11
ORD IDord-0d821eb87dee43209886bb2860a69f69
Source noteuspto-grants-1999_11