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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892860Generated: October 30, 2026

Pyridine → HCID 19894147, compound

https://huagongshe.com/reaction/892860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantHCID 21684721HCID 21684721—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 19894147HCID 1989414766.3%

Reaction Steps

To a solution of trans-3-(3-(4-hydroxyphenoxy)phenyl)propenoic acid (26.22 g, 102.4 mmol) in CH2Cl2 (500 mL) at 0° C., was added iso-butylchloroformate (29.38 g, 215.1 mmol) followed by the dropwise addition of triethylamine (21.73 g, 215.1 mmol). Upon completion of addition, the cooling bath was removed and the reaction allowed to warm to r.t. and stirred for 1 hr. N,O-dimethylhydroxylamine hydrochloride (11.99 g, 122.9 mmol) was then added followed by the dropwise addition of pyridine (19.44 g, 245.8 mmol) and the reaction was stirred for 30 mins. It was then diluted with brine (500 mL) and the layers were separated. The aqueous was extracted with CH2Cl2 (2×500 mL). The organics were combined, dried with MgSO4 and concentrated. The resulting residue was chromatographed (silica gel, ether:hexanes, 1:1) to afford trans-N-methoxy-N-methyl-3-(3-(4-iso-butyloxycarboxyphenoxy)phenyl)propenamide (27.13 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120752
Source datasetuspto-grants-1992_06
ORD IDord-9953e4b9a074499e86cea848accb0aee
Source noteuspto-grants-1992_06