Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583512Generated: November 1, 2026

3-Pyridinemethanol → HCID 20159236, compound

https://huagongshe.com/reaction/1583512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinemethanolHCID 7510—
ReactantThiiraneHCID 9865—
ReactantTrifluoromethanesulfonic acidHCID 62406—
SolventWaterHCID 962—
ProductHCID 20159236HCID 2015923694%

Reaction Steps

Trifluoromethanesulfonic acid (1.327 mL, 0.015 mol) was added dropwise to 3-pyridinemethanol (2.91 mL, 0.030 mol), followed by ethylene sulfide (0.89 mL, 0.015 mol). The resulting homogeneous mixture was heated (oil bath) at 50°-70° C. under N2 for 20 h. The reaction mixture was then taken up in H2O (15 mL) and extracted with CH2Cl2 (5×5 mL). The aqueous phase was concentrated in vacuo and then applied to a C18 reverse-phase column. Elution with H2O followed by evaporation of the relevant fractions gave a pale yellow oil. This material was rechromatographed to give a nearly colourless oil. After drying in vacuo (P2O5) this afforded the product (4.50 g, 94%) as a viscous oil. ir (film) νmax : 3450 (s, OH), 2560 (w, SH) cm-1 ; 1Hmr (d6 -acetone)δ: 9.10-8.05 (m, 4H, aromatic), 5.01 (t, J= 5.5 Hz, 2H, N-CH2), 4.93 (s, 2H, --CH2OH), 4.43 (br S, 1H, -OH), 3.43-3.18 (m, 2H, S-CH2), 2.34-2.10 (m, 1H, SH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552696
Source datasetuspto-grants-1985_11
ORD IDord-fed7c253f2b343c7893534fb1067e1e9
Source noteuspto-grants-1985_11