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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250464Generated: October 30, 2026

Methanol → HCID 18326277, compound

https://huagongshe.com/reaction/1250464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 53777615HCID 53777615—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18326277HCID 1832627795%

Reaction Steps

A solution of 3-Chloro-4-(4-nitrilo-butoxy)-benzoic acid methyl ester (6.24 g, 24.6 mmol in THF (100 ml) and methanol (100 ml) was treated with 5 N sodium hydroxide solution (35 ml) with stirring at room temperature for 1 h. The reaction mixture was concentrated in vacuo, diluted with water, and acidified to pH 1 with 5 N hydrochloric acid. The resulting suspension was extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered, and concentrated in vacuo. The resulting off white solid was triturated with hot petroleum ether, cooled and filtered to give 5.58 g (95%) of the title compound as a white solid mp 150° C.; 1H NMR (CDCl3) δ2.22-2.28 (m, 2H), 2.69 (t, J=7.0 Hz, 2H), 3.90 (s, 3H), 4.23 (t, J=5.5 Hz, 2H), 6.97 (d, J=8.6 Hz, 1H), 8.01 (dd, J=8.6, 2.2 Hz, 1H), 8.14 (d, J=2.0 Hz, 1H). IR (KBr) 3400, 2200, 1700, 1600, 1450, 1275 and 1050 cm−1, mass spectrum (EI), m/z 239/241. Anal. Calcd. for C11H10ClNO3: C, 55.13; H, 4.21; N, 5.85. Found: C, 54.84; H, 4.01; N, 5.69.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339064B1
Source datasetuspto-grants-2002_01
ORD IDord-31db4140861f4379858a1a4f4d71aa36
Source noteuspto-grants-2002_01