HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380367Generated: November 1, 2026
Tris(hydroxymethyl)aminomethane → HCID 178511423, compound
https://huagongshe.com/reaction/2380367
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tris(hydroxymethyl)aminomethane | HCID 6503 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 178520549 | HCID 178520549 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178511423 | HCID 178511423 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05366993 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-aa4606097da249a1befbbe119da27ac5 |
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| Source note | uspto-grants-1994_11 |
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