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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640028Generated: November 2, 2026

Hydrochloric Acid → HCID 57429435, compound

https://huagongshe.com/reaction/1640028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantThionyl ChlorideHCID 24386—
Reactant7-METHYL-2,3-DIHYDRO-1,4-BENZODIOXINE-6-CARBOXYLIC ACIDHCID 16766586—
SolventEthanolHCID 702—
ProductHCID 57429435HCID 5742943589%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 7-methyl-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylic acid (1.72 g, 8.8 mmol) in ethanol (100 mL) was cooled to 0° C. and stirred for 1 h prior to dropwise addition of thionyl chloride (3.9 mL, 53.2 mmol) over 1 h. After this time, the mixture was warmed to room temperature for 1 h, then transferred to an oil bath, and heated to 70° C. overnight. The mixture was then cooled to room temperature and 2 N hydrochloric acid (50 mL) added slowly followed by diethyl ether (50 mL). The aqueous layer was extracted twice with diethyl ether (50 mL), the combined organic layers washed with brine (100 mL), dried over magnesium sulfate, and concentrated under reduced pressure to afford ethyl 7-methyl-2,3-dihydrobenzo[b][1,4]dioxine-6-carboxylate (1.7 g, 89%) as a white solid: 1H NMR (500 MHz, CDCl3) δ 7.51 (s, 1H), 6.70 (s, 1H), 4.30 (q, J=7.0, 7.5 Hz, 2H), 4.26 (m, 4H), 2.49 (s, 3H), 1.36 (t, J=7.0, 7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110681B2
Source datasetuspto-grants-2012_02
ORD IDord-f0eb801e6eb14382b49be7960e32cbf6
Source noteuspto-grants-2012_02