Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258775Generated: October 30, 2026

Diisopropyl Ether → HCID 21426472, compound

https://huagongshe.com/reaction/258775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantPotassium thiocyanateHCID 516872—
ReactantSodium BicarbonateHCID 516892—
ReactantSodiumHCID 5360545—
ReactantHCID 21426457HCID 21426457—
ReactantHCID 178527916HCID 178527916—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21426472HCID 2142647242.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

The sodium salt of 3-acetoxymethyl-2-carboxy-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (10 g.) is dissolved in water (51 cc.). Potassium thiocyanate (60 g.), sodium bicarbonate (2.24 g.) and 1-phenyl-5-thioxo-1,2,3,4-tetrazoline (4.75 g.) are added to this solution and the mixture is heated to 60° C. for 8 hours. After cooling, the reaction mixture is diluted with water (250 cc.) and washed with ethyl acetate (200 cc.) after acidification to pH 5.5 by adding 4 N hydrochloric acid. The mixture is then acidified to pH 1.5 by adding 4 N hydrochloric acid in the presence of ethyl acetate (100 cc.). After decanting the organic phase, the aqueous phase is extracted four times with ethyl acetate (a total of 400 cc.). The organic extracts are combined, washed three times with an 0.1 N hydrochloric acid solution (a total of 300 cc.) and then twice with water (a total of 300 cc.), dried over sodium sulphate, treated with decolourising charcoal, filtered and then concentrated to dryness under reduced pressure (20 mm Hg). The residue obtained is dissolved in tetrahydrofuran (50 cc.) and this solution is then added to isopropyl ether (1 liter). A product precipitates, which is isolated by filtration and dried under reduced pressure (0.1 mm Hg). 2-Carboxy-8-oxo-7-[(1,3-dithiol-2-on-4-yl)-acetamido]-3-[(1-phenyl-1,2,3,4-tetrazol-5-yl)-thiomethyl]- 5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (5.4 g.) is thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034090
Source datasetuspto-grants-1977_07
ORD IDord-0dd15a0a469f4b86af5bccf3b42e1a0c
Source noteuspto-grants-1977_07