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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097625Generated: November 1, 2026

Sodium Sulfate → HCID 178522150, compound

https://huagongshe.com/reaction/2097625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantLithium borohydrideHCID 4148881—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58941813HCID 58941813—
ReactantHCID 178509299HCID 178509299—
CatalystAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 178522150HCID 17852215085%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of N-(3-chloro-4-fluorophenyl)-4-formyl-1,2,5-oxadiazole-3-carboxamide (4.5 g, 17 mmol) in THF (75 mL) was added 5-aminotetrazole (4.26 g, 50.1 mmol), sodium sulfate (1.0 g, 8.0 mmol) and acetic acid (50 μL, 0.80 mmol). The resulting mixture was stirred at 40° C. for 36 h, and then an additional 20 mL THF was added followed by sodium tetrahydroborate (947 mg, 25 mmol). After stirring for 3 h, lithium tetrahydroborate (545 mg, 25.0 mol) was added to the reaction solution and stirred overnight. The reaction solution was diluted with 1 N NaOH solution. The aqueous layer was separated and acidified with 6 N HCl to pH 1. A white solid precipitated out of solution and was filtered to afford the desired product (4.82 g, 85%). LCMS for C11H9ClFN8O2(M+H)+: m/z=339.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450351B2
Source datasetuspto-grants-2013_05
ORD IDord-641e8caa1722415c89e260219553eb0e
Source noteuspto-grants-2013_05