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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610729Generated: November 3, 2026

Sodium borohydride → HCID 22261585, compound

https://huagongshe.com/reaction/1610729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22261823HCID 22261823—
CatalystZincchlorideHCID 3007855—
SolventDiethyl EtherHCID 3283—
ProductHCID 22261585HCID 2226158576.3%

Reaction Steps

To a suspension (50 ml) of zinc chloride (3.41 g, 25 mmol) in ether was added sodium borohydride (1.89 g, 50 mmol) at room temperature, and the mixture was stirred as it was for 2 hrs. Insoluble material was filtered off. To the filtrate was added a solution of ethyl 3-oxo-3-(2-phenyl-1,3-thiazol-4-yl)-2-[3-(1,1,2,2-tetrafluoroethoxy)benzyl]propionate (6.01 g, 12.5 mmol) in ether (40 ml) under ice-cooling, and the mixture was stirred as it was for 1 hr. The reaction was quenched with 1N hydrochloric acid. The mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=6:1, 4:1) to give ethyl 3-hydroxy-3-(2-phenyl-1,3-thiazol-4-yl)-2-[3-(1,1,2,2-tetrafluoroethoxy)benzyl]propionate (4.61 g, 76%) as a colorless transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-01abeb2991a848ebb444126c9a69be05
Source noteuspto-grants-2006_01