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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005538Generated: October 31, 2026

2-(5-(3,5-Dichlorophenylthio)-4-isopropyl-1-methyl-1H-imidazol-2-yl)ethanol → 2-[2-(Cyclododecen-1-yloxyl)ethyl]-5-(3,5-dichlorophenylthio)-4-isopropyl-1-methyl-1H-imidazole

https://huagongshe.com/reaction/1005538

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-(3,5-Dichlorophenylthio)-4-isopropyl-1-methyl-1H-imidazol-2-yl)ethanolHCID 474010—
Reactant1-MethoxycyclododeceneHCID 520016—
Product2-[2-(Cyclododecen-1-yloxyl)ethyl]-5-(3,5-dichlorophenylthio)-4-isopropyl-1-methyl-1H-imidazoleHCID 5412958982%

Reaction Steps

The compound 22 (345 mg, 1 mmol) was converted to the enol ether with 1-methoxycyclododecene (982 mg, 5 mmol) in the same manner as the example 41 to give the compound 49 (418 mg, 82%). Mp 96-102° C. PMR (CDCl3 -0.1% d5 -Py): δH1.24 (6 H, d, J 7 Hz, (CH3)2C), 3.11 (2 H, t, J 6.2 Hz, CH2 -Im), 3.10 (1 H, m, (CH3)2CH), 3.51 (3 H, s, NCH3), 3.96 (2 H, t, J 6.2 Hz, OCH2), 4.36 (1 H, t, J 7.8 Hz, =CH), 6.80 (2 H, d, J 1.6 Hz, arom-H), 7.10 (1 H, t-like, arom-H). IR(KBr)cm-1 : 3434, 3057, 1702, 1662, 1566, 1558, 1469, 1409, 1378, 1235, 1130. Elementary analysis (for C27H38N2Ocl2S) Calcd. : C, 63.64% H, 7.52% N, 5.50% S, 6.29% Cl, 13.91% Found: C, 64.48% H, 7.69% N, 5.10% S, 6.03% Cl, 12.85%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054591
Source datasetuspto-grants-2000_04
ORD IDord-a106849d081b4286ac5de935bbf99958
Source noteuspto-grants-2000_04