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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387641Generated: October 30, 2026

Formaldehyde → HCID 59463923, compound

https://huagongshe.com/reaction/2387641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68500709HCID 68500709—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59463923HCID 59463923—

Reaction Steps

Preparation of 2-(2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-[2,5-c]pyridine: To a solution of 2-(2-(2-(tert-butyldiphenylsilyloxy)ethyl)-5-(2,5-difluorophenyl)-2-phenyl-1,3,4-thiadiazol-3(2H)-yl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine (0.157 g, 0.225 mmol) in 5 mL DCE was added formaldehyde (0.067 mL, 37 wt % in water, 0.901 mmol) followed by sodium triacetoxyborohydride (0.052 g, 0.248 mmol). The resulting suspension was stirred vigorously at room temperature overnight, then treated with saturated Na2CO3 solution (30 mL) and stirred for 10 minutes. The mixture was extracted with EtOAc (3×30 mL) and the combined organic phases were washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography (0-1% MeOH/DCM) to afford the desired product as a bright yellow foam, 0.119 g, 74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268871B2
Source datasetuspto-grants-2012_09
ORD IDord-cc0ddf6f1f1f4ab79158037e9210e7c8
Source noteuspto-grants-2012_09