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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615664Generated: October 29, 2026

HCID 20426825, compound → HCID 20426832, compound

https://huagongshe.com/reaction/615664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20426825HCID 20426825—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-phenyltetrazole-5-thiolHCID 178527986—
SolventDimethylformamideHCID 6228—
ProductHCID 20426832HCID 20426832—

Reaction Steps

To 300 ml of dried dimethylformamide, was added 5.6 g (0.05 mol.) of potassium tert-butoxide and 8.9 g (0.05 mol.) of 1-phenyl-5-mercaptotetrazole. The mixture was stirred for 20 minutes at room temperature. Thereafter, to the mixture which was cooled to 5° C. and kept there, was added gradually dropwise a solution prepared by adding 13 g (0.04 mol.) of 3-chloro-3-(2,4-dichlorophenyl)phthalide in 75 ml of dried dimethylformamide. After dropwise addition, the cooling bath was removed, and the mixture was stirred for 5 hours at room temperature. Thereto, 300 ml of a saturated aqueous solution of ammonium chloride was added. The reaction mixture was extracted with ethyl acetate repeatedly. The extract was washed with water, and the resulting organic layer was dried over anhydrous sodium sulfate. Sodium sulfate was filtered off with suction, and the filtrate was concentrated to yield 23.5 g of oily substance. This oily substance was separated and purified by flash column chromatography (silica gel: 800 g, eluate: hexane-ethyl acetate (3:1 by volume) mixture). Thus, the intended compound, 3-(1-phenyl-tetrazole-5-ylthio)-3-(2,4-dichlorophenyl)phthalide (3), was obtained in a form of white crystals. Yield 7.8 g, Melting Point 148° to 149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500636
Source datasetuspto-grants-1985_02
ORD IDord-727015ac7c3449c5a1a5dce68db7ce58
Source noteuspto-grants-1985_02