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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380367Generated: November 1, 2026

Tris(hydroxymethyl)aminomethane → HCID 178511423, compound

https://huagongshe.com/reaction/2380367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantPotassium BromideHCID 253877—
ReactantHCID 178520549HCID 178520549—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178511423HCID 178511423—

Reaction Conditions

Temperature70 °C

Reaction Steps

To 0.8 g (2.3 mmol) of 3-(4-cyclododecyl-1-oxobutyl)-4-hydroxy-2-(5H)thiophenone in 20 mL of ethanol at 70° C. is added 0.26 g (2.2 mmol) of trishydroxymethyl aminomethane dissolved in 5 mL of water. The reaction mixture is stirred at 70° C. for 0.5 hours and then the solvents are evaporated. The residue is recrystallized from tetrahydrofuran/ether (2:1) to give 0.66 g of an off white solid: m.p. 141°-144° C.; IR (KBr) 3420, 2920, 2830, 1580 cm-1 ; NMR (DMSO-d6) δ1.11.-1.4 (m, 10H), 2.55 (t, J=7 Hz, 2H), 3.26 (s, 1H), 3.31 (s, 4H), 3.47 (d, J=5, 3 Hz), 5.15 (t, J=5 Hz, 2H), 7.6 (bs, 2H); MS (DCI) [M+H]+ 353. Anal. Calc' d. for C4H43NO6S: C 60.86; H 9.15; N, 2.96 Found: C, 60.91; H 9.16; N, 2.88

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05366993
Source datasetuspto-grants-1994_11
ORD IDord-aa4606097da249a1befbbe119da27ac5
Source noteuspto-grants-1994_11