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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065925Generated: November 3, 2026

Tetrahydrofuran → HCID 131712743, compound

https://huagongshe.com/reaction/1065925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium Acetate TrihydrateHCID 23665404—
ReactantHCID 131712744HCID 131712744—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 131712743HCID 13171274368.1%

Reaction Steps

7-[2-Cyclopentyloxyimino-2-{2-(2,2,2-trifluoroacetamido)thiazol-4-yl}acetamido]-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (2.8 g) was added to a solution of sodium acetate trihydrate (5.8 g) in water (25 ml), and tetrahydrofuran (8.0 ml) was added thereto to give clear solution. The solution was stirred for 16 hours at ambient temperature. To the reaction mixture were added water and ethyl acetate and the mixture was adjusted to pH 6.2 with a saturated aqueous solution of sodium bicarbonate. The separated aqueous layer was washed twice with ethyl acetate and adjusted to pH 3.0 with 10% hydrochloric acid. Precipitates were collected by filtration, washed with water and dried under reduced pressure to give 7-[2-cyclopentyloxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(1-methyl-1H-tetrazol-5yl)thiomethyl-3-cephem-4-carboxylic acid (syn isomer) (1.63 g), mp 152° to 154° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04331664
Source datasetuspto-grants-1982_05
ORD IDord-70813d0edb5e4f38a2d9331521803ad5
Source noteuspto-grants-1982_05