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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257581Generated: November 3, 2026

Chloroacetyl chloride → HCID 16495703, compound

https://huagongshe.com/reaction/1257581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant2,4-DimethoxybenzylamineHCID 597250—
SolventTetrahydrofuranHCID 8028—
ProductHCID 16495703HCID 1649570391%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2,4-dimethoxybenzylamine (1.50 mL, 10.0 mmol) and triethylamine (2.00 mL, 14.3 mmol) in tetrahydrofuran (20 mL) at 0° C. was added chloroacetyl chloride (0.80 mL, 10 mmol). The reaction was then stirred at 0° C. for three hours. The crude reaction mixture was partitioned between ethyl acetate and water, and the organic layer dried over brine and magnesium sulfate, filtered, and evaporated in vacuo to yield 2.2074 g (91%) of N-(2,4-Dimethoxy-benzyl)-2-chloro-acetamide which was carried forward without purification. LCMS (Method E, ESI): RT=1.43 min, m+H=244.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461328B2
Source datasetuspto-grants-2013_06
ORD IDord-311de4145aa8459984ba50883da33acb
Source noteuspto-grants-2013_06