Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512788Generated: November 2, 2026

Hydrochloric Acid → 5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carbohydrazide

https://huagongshe.com/reaction/512788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN'-(5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)hydrazinecarboxylic acid 4-methoxy-benzyl esterHCID 59838614—
Solvent1,4-DioxaneHCID 31275—
Product5-Methyl-2,3-dihydro-1,4-benzodioxine-6-carbohydrazideHCID 1576755443.3%

Reaction Steps

In a 500 mL volume flask, was combined 18.6 g (0.0499 moles) of N′-(5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)-hydrazinecarboxylic acid 4-methoxy-benzyl ester, 72 mL of concentrated HCl, and 108 mL of dioxane. The flask was placed into an 80° C. oil bath and mechanically stirred for 2 hours. The reaction mixture was cooled with ice water, then poured onto ice water and transferred to a separatory funnel. The reaction mixture—H2O solution was then extracted twice with 150 mL of CH2Cl2 to remove the acids and neutrals (the starting material). The aqueous phase was made basic (pH 12) with a 20% NaOH solution and extracted 4 times with 150 mL of ethyl acetate. The ethyl acetate extract was dried over MgSO4 and concentrated to yield 4.5 g of 5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid hydrazide. 1H NMR (CDCL3, 300 MHz) δ (ppm): 7.0 (s, 1H), 6.85 (d, 1H), 6.74 (d, 1H), 4.28 (m, 4H), 2.781 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102648B1
Source datasetuspto-grants-2015_08
ORD IDord-a5437375b27644b18ada3c48053ffeca
Source noteuspto-grants-2015_08