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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973947Generated: October 30, 2026

Acetic Anhydride → HCID 67924983, compound

https://huagongshe.com/reaction/973947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 131717082HCID 131717082—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67924983HCID 6792498370.5%

Reaction Steps

Methyl-3-(4-pyridinyl)alanine, dihydrochloride (1.4 g, 0.0053 mol) is stirred in dry tetrahydrofuran (20 mL) with acetic anhydride (0.9 mL, 0.0095 mol) and triethylamine (3.3 mL, 0.0233 mol) at room temperature. After stirring at room temperature overnight the mixture is diluted with 20 mL tetrahydrofuran and filtered and the solids washed with tetrahydrofuran. The filtrate is concentrated to a dark oil, dissolved in dichloromethane (50 mL) and washed with dilute sodium bicarbonate solution (50 mL). The organic layer is dried over magnesium sulfate and concentrated. The residue is triturated with diethyl ether, filtered, and dried to afford 0.83 g of the title compound as a tan solid; mp 86-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066662
Source datasetuspto-grants-1991_11
ORD IDord-c8d965055175402d9e915464d654c559
Source noteuspto-grants-1991_11