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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734797Generated: November 1, 2026

Cyclopentanone → HCID 11619765, compound

https://huagongshe.com/reaction/734797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanoneHCID 8452—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 69065035HCID 69065035—
CatalystAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11619765HCID 11619765—

Reaction Steps

A mixture of 80.6 mg (0.20 mmol) of (2-{4-[5-(4-chlorophenyl)pyridin-2-ylethynyl]phenoxy}ethyl)cyclopropylmethylamine, 35 μL (0.40 mmol) of cyclopentanone, and one drop of AcOH in 10 mL of THF was stirred for 15 minutes. 169.5 mg (0.80 mmol) of sodium triacetoxyborohydride was added and the mixture was stirred for 24 hours at RT. A further 17.5 μL of cyclopentanone and 85 mg of sodium triacetoxyborohydride were added and the mixture was again stirred for 24 hours at RT. The reaction mixture was diluted with water, made basic with saturated aqueous potassium carbonate solution, and the aqueous phase was extracted with EtOAc. The combined organic phases were dried over sodium sulfate and evaporated down in vacuo. The crude product was purified by column chromatography (silica gel, EtOAc/MeOH/conc. aqueous ammonia 98:2:0.2) and stirred with DIPE. Yield: 22 mg (23% of theoretical); C30H31ClN2O (M=471.033); calc.: molpeak (M+H)+: 471/473 (Cl); found: molpeak (M+H)+: 471/473 (Cl); HPLC-MS: 5.83 minutes (method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592358B2
Source datasetuspto-grants-2009_09
ORD IDord-b9a5ad4193e344839ac097b0b9c67ffa
Source noteuspto-grants-2009_09