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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260889Generated: October 31, 2026

Acetic Acid → HCID 44366862, compound

https://huagongshe.com/reaction/2260889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 22844873HCID 22844873—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44366862HCID 4436686273.2%

Reaction Steps

A mixture of 16 (50 mg, 0.1 mmol), acetic acid (7 μL, 0.12 mmol), and 0.17 mL of 1M tetrabutylammonium fluoride in THF (0.17 mmol) was stirred in 10 mL tetrahydrofuran overnight. Water (2 mL) and 15 mL ethyl ether were added followed by stirring for 5 minutes. The organic phase was extracted with 2 mL water and then the combined aqueous solution was washed with 15 mL ethyl ether. The aqueous extract was concentrated in vacuo to 1 mL and then applied to a 4-mL Dowex 1×4 100-200 (-3OH) column to remove tetrabutylammonium salts by eluting with water followed by 20% aqueous methanol. The solvent was removed in vacuo and the product was recrystallized from ethanol/ethyl acetate to afford 19.5 mg (54%) of 17; mp. 187°-90° C. dec; FAB MS 267 (M+H)+ ; 1H NMR (DMSO-d6) δ 8.0 (s, 1, H-8), 6.68 (br, s, 2, NH2), 5.95 (m, 1, I'-H), 5.71 (brs, 2, NH2), 5.22 (m, 1, 5'-OH), 3.73 (m, 1, 5'-H), 3.57 (m, 2, 4'-H, 5'-H), 2.4 (m, 1, 2'-H), 2.32 (m, 1, 2'-H), 2.12 (m, 1, 3'-H), 1.98 (m, 1, 3'-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478928
Source datasetuspto-grants-1995_12
ORD IDord-2b15bd030f194f75b6c9f4ca14224b7c
Source noteuspto-grants-1995_12