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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272556Generated: November 1, 2026

Acetone → HCID 68454739, compound

https://huagongshe.com/reaction/272556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68454615HCID 68454615—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 68454739HCID 6845473974%

Reaction Steps

A mixture of 0.2 g (1 mmol) 5-(pyrrolidin-3-ylamino)-1H-indole-2-carboxylic acid ethyl ester, 0.042 g (1 mmol) acetone and 0.1 ml acetic acid in 10 ml THF was treated after 1 h with 0.233 g (1 mmol) sodium trisacetoxyborohydride at 0° C. The mixture was allowed to react for 39 h at room temperature. The mixture was treated with 5 ml water, 15 ml Na2CO3 aq. and 15 ml ethyl acetate and the aqueous phase was extracted with 40 ml ethyl acetate. The combined organic phases were dried over Na2SO4, filtered and evaporated to dryness. The residue was purified over silica eluting with a gradient formed from DCM/2N NH3 in methanol to yield 0.17 g (74%) of the title compound and light brown solid. MS (m/e): 316.3 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456174B2
Source datasetuspto-grants-2008_11
ORD IDord-fd971e5449574af2a645338234bff2e4
Source noteuspto-grants-2008_11