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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031042Generated: October 26, 2026

Tetrahydrofuran → HCID 14460289, compound

https://huagongshe.com/reaction/1031042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-Nitrobenzyl bromoacetateHCID 7015321—
ReactantHCID 19905241HCID 19905241—
SolventDimethylformamideHCID 6228—
ProductHCID 14460289HCID 14460289—

Reaction Conditions

Temperature-30 °C

Reaction Steps

14.4 ml of 1 N solution of lithium bis-trimethylsilylamide in tetrahydrofuran (THF) are added dropwise with stirring at -70° C. to a solution of 1.91 g (12 mmol) of tert-butylthioazetidin-2-one in 6 ml of dry N,N-dimethylformamide (DMF) and then a solution of 4.93 g (18 mmol) of p-nitrobenzyl bromoacetate in 6 ml of DMF is added dropwise to the mixture and the mixture is stirred at -30° C. for a further 30 minutes. Dilution of the reaction mixture with 100 ml of toluene, washing with three portions of 50 ml each of water, drying the organic phase over magnesium sulphate and evaporating the solvent in vacuo yields 4.3 g of solid crude product, which is chromatographed on 120 g of silica gel using toluene/ethyl acetate (4:1). The purified product (2.6 g) is recrystallized from 100 ml of dry isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05108747
Source datasetuspto-grants-1992_04
ORD IDord-39555710e1bc46829693a0f4ad1f1377
Source noteuspto-grants-1992_04