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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039615Generated: October 31, 2026

Hydrochloric Acid → HCID 57855931, compound

https://huagongshe.com/reaction/2039615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
Reactant3-Chloro-2,4-difluoro-5-nitrobenzoic acidHCID 15549918—
CatalystMethylamineHCID 6329—
SolventWaterHCID 962—
ProductHCID 57855931HCID 57855931102.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 5 g (21.05 mmol) of 3-chloro-2,4-difluoro-5-nitro-benzoic acid (known from WO 03/077914) in 50 mL of H2O is cooled to a temperature of 0° C. Then 5.86 ml (42.10 mmol) of triethylamine were added dropwise followed by the dropwise addition of 1.82 ml (21.05 mmol) of methylamine (40% in H2O). After 30 min of stirring at 0° C., 0.18 ml (2.11 mmol) of methylamine (40% in H2O) is added and the mixture is stirred again during 30 min at a temperature of 0° C. The pH of the mixture is adjusted to 1-0.5 by the addition of concentrated HCl at a temperature of 0° C. The product is extracted with tert-butyl methyl ether (2 times) and the organic phase is washed once with brine, dried on Na2SO4, filtrated and the solvent is evaporated. 5.35 g (21.52 mmol, 102%) of a crude yellow solid were obtained and used directly in the next step without purification. LC/MS: 247/249 (M−1)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580785B2
Source datasetuspto-grants-2013_11
ORD IDord-c6e2d1c1f97d4b8bb389489de4a9808b
Source noteuspto-grants-2013_11