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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544264Generated: October 31, 2026

Ethylmorpholine → HCID 70519969, compound

https://huagongshe.com/reaction/544264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Adamantaneacetic acidHCID 123221—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 70519969HCID 70519969—

Reaction Steps

A mixture of 4.8 g (0.02 m) of L-proline benzyl ester hydrochloride, 3.88 g (0.02 m) of α-(1-adamantyl)acetic acid, 5.4 g (0.04 m) of 1-hydroxybenzotriazole, 2.56 ml of N-ethylmorpholine, 60 ml of dimethylformamide and 4.16 g (0.02 m) of dicyclohexylcarbodiimide was stirred overnight at 25°. The mixture was filtered and the tetrahydrofuran removed in vacuo from the filtrate to leave a residue which was taken up in 200 ml of ethyl acetate. The resulting extract was acidified with dilute hydrochloride acid. The layers were separated. The organic layer was extracted several times with ethyl acetate. The organic extracts were combined and washed with dilute acid, water, bicarbonate solution and brine then dried and evaporated to give an amber syrup of N-(1-adamantyl)-ethanoylproline benzyl ester, m/e=381. A second run on a 0.04 m scale gave 16.2 g of ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448972
Source datasetuspto-grants-1984_05
ORD IDord-fde631c0bc3e4dd7a4987c5a0484bb0f
Source noteuspto-grants-1984_05