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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206810Generated: November 3, 2026

Sodium borohydride → HCID 86714100, compound

https://huagongshe.com/reaction/2206810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86714098HCID 86714098—
SolventHydrochloric AcidHCID 313—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 86714100HCID 8671410091.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-chloro-6-(4-ethoxybenzyl)-4-((3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzofuran-3(2H)-one (285 mg, 0.345 mmole) in THF/MeOH (9 mL/3 mL) was added NaBH4 (39.2 mg, 1.04 mmole) at 0° C. The resulting solution was stirred at 0° C. for 1 hr, diluted with 1N—HCl and extracted with ethyl acetate. The organic layer was washed with water then brine, dried over MgSO4, filtered, and concentrated in vacuo. The crude residue was purified on Biotage® purification apparatus to yield the title compound (260 mg, 91%) as a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-baea30b5f8d74ced9cbc1917a07ba30f
Source noteuspto-grants-2016_06