Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922400Generated: October 31, 2026

Hydrochloric Acid → 5-(Benzyloxy)-2-methoxybenzamide

https://huagongshe.com/reaction/922400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
Reactant5-(Benzyloxy)-2-methoxybenzoic AcidHCID 13282047—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product5-(Benzyloxy)-2-methoxybenzamideHCID 2150442363%

Reaction Steps

To a stirred solution of 5-(benzyloxy)-2-methoxybenzoic acid (8, 1.16 g. 4.5 mmol) in CH2Cl2 (25 mL) at room temperature was added oxalyl chloride (1.5 mL, 17.9 mmol). The reaction mixture was stirred at room temperature for 2 h. It was concentrated to dryness to provide the crude acid chloride as a brown-yellow waxy solid. The crude acid chloride was dissolved in THF (10 mL) and was added dropwise to a stirred mixture of concentrated NH4OH (20 mL) and THF (10 mL) at 0° C. The reaction mixture was warmed to room temperature and stirred for 1 h and was adjusted to pH 8 with 2 N HCl. The precipitate was collected, washed with water, and dried in vacuo to afford the title compound (0.73 g, 63%) as a white solid: 1H NMR (500 MHz, CDCl3) δ 7.88 (d, J=3.3 Hz, 1H), 7.82 (br s, 1H), 7.47-7.43 (m, 2H), 7.40-7.37 (m, 2H), 7.33-7.30 (m, 1H), 7.10 (dd, J=9.0, 3.3 Hz, 1H), 6.94 (d, J=9.0 Hz, 1H), 5.75 (br s, 1H), 5.08 (s, 2H), 3.94 (s, 3H); ESI MS m/z 258 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278940B2
Source datasetuspto-grants-2016_03
ORD IDord-e56e933fe70e44d98bde925c39c74a27
Source noteuspto-grants-2016_03