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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335675Generated: October 30, 2026

Water → HCID 57751156, compound

https://huagongshe.com/reaction/335675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dimethylbenzoyl ChlorideHCID 81088—
ReactantHCID 57751170HCID 57751170—
SolventDichloromethaneHCID 6344—
ProductHCID 57751156HCID 5775115678.6%

Reaction Steps

To a solution of (R)-3-methoxy-2-methyl-benzoic acid N′-(1-cyclohexyl-but-3-enyl)-hydrazide (1.3 g, 4.11 mmol) in CH2Cl2 (5 mL), was added K2CO3 (2.27 g, 16.44 mmol), H2O (5 mL), and finally 3,5-dimethylbenzoyl chloride (727 mg, 4.31 mmol). The reaction was stirred at room temperature for 24 h. Additional CH2Cl2 and H2O were added to aid manipulation, the CH2Cl2 layer was separated, and the aqueous layer was extracted with CH2Cl2. The CH2Cl2 solutions were combined and dried over anhydrous Na2SO4. The solvent was evaporated in vacuo and the residue was purified by flash chromatography to provide (R)-3,5-dimethyl-benzoic acid N-(1-cyclohexyl-but-3-enyl)-N′-(3-methoxy-2-methyl-benzoyl)-hydrazide as a white solid (1.45 g, 78% yield). Rf=0.21 (3:1 EtOAc:n-Hexane); 1H NMR (400 MHz, DMSO-d6) δ 10.47+10.39 (2s, 1H), 7.20-7.01 (m, 5H), 6.37 (d, J=7.2 Hz, 1H), 6.22-5.89 (m, 1H), 5.18 (dd, 1H), 5.02 (dd, 1H), 4.46 (m, 1H), 3.79 (s, 3H), 2.44-2.34 (m, 2H), 2.29 (s, 3H), 2.02-1.53 (m, 8H), 1.26-1.02 (m, 3H); HRMS (ESI) m/z calcd for C28H37N2O3 [M+H]+ 449.2804. found 449.2793, calcd for C28H36N2NaO3 [M+Na]+ 471.2624. found 471.2615.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08884060B2
Source datasetuspto-grants-2014_11
ORD IDord-d578d26668b5440d8412520c38d8255b
Source noteuspto-grants-2014_11