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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400313Generated: October 28, 2026

Sodium borohydride → HCID 68276152, compound

https://huagongshe.com/reaction/1400313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59054370HCID 59054370—
ReactantHCID 68276186HCID 68276186—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68276152HCID 6827615291.6%

Reaction Steps

A microwave vial was charged with 2,2-difluoro-2-[(1-fluoronaphthalen-2-yl)oxy]-N-(furan-2-ylmethyl)acetamide (60 mg, 0.18 mmol), sodium borohydride (16 mg, 0.41 mmol) and 2 mL of dry THF. To this mixture, a solution of 12 (51 mg, 0.20 mmol) in 1 mL of dry THF was added. The vial was sealed and placed in the microwave reactor and irradiated for 30 min at 110° C. until the starting materials had been completely consumed as judged by TLC (petroleum ether/ethyl acetate 80:20). The mixture was evaporated under reduced pressure and the crude was purified by preparative HPLC to afford 2,2-difluoro-2-[(1-fluoronaphthalen-2-yl)oxy]-N-(furan-2-ylmethyl)ethanamine as orange oil (53 mg, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906946B2
Source datasetuspto-grants-2014_12
ORD IDord-6defbabff79b446da9a8c5efd9197ba3
Source noteuspto-grants-2014_12