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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226243Generated: October 30, 2026

Triethylamine → HCID 10796970, compound

https://huagongshe.com/reaction/226243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromoacetonitrileHCID 11534—
ReactantPiperidin-2-ylmethanolHCID 94263—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10796970HCID 10796970—

Reaction Steps

The method follows that of S3 using 2-piperidinemethanol (26.50 g, 0.230 mol), BrCH2CN (30.35 g, 0.253 mol), Et3N (35.27 mL, 0.253 mol) and dry THF (150 mL). The crude product was purified by flash chromatography using ether/CH3OH (19:1) as eluent. The title-compound was crystallised from ether yielding cream-coloured crystals (31.46 g, 89%). δH(250 MHz; CDCl3); 1.2-1.85 (m, 6H, NCH2CH2CH2, CH2CH2CH2CH and CH2CH2CH), 2.05 (s (broad), 6H, OH), 2.4 (m, 1H, NCH2CH2), 2.55 (3×d, 1H. 1×NCH2CH2), 2.95 (m, 1H, NCHCH2), 3.45 (d, 1H, J=17 Hz, 1×NCH2CN), 3.5 (2×d, 1H, J=3 Hz and 12 Hz, 1×CHCH2OH), 3.76 (2×d, 1H, J=3 Hz and 12 Hz, CHCH2OH) and 4.05 (d, 1H, J=17 Hz, 1×NCH2CN); δC (62.9 MHz; CDCl3); 23.71, 25.25, 28.69, 43.43, 54.04, 60.73, 64.46 and 115.05 (CN); FAB MS, m/z(M+H)+ 155; IR υmax/cm−1; 3400 (OH, m broad), 2350 and 2240 (CN) and 1650.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557215B2
Source datasetuspto-grants-2009_07
ORD IDord-b9e1342bbe4d452a8326e3dceb63bb27
Source noteuspto-grants-2009_07