Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580157Generated: November 1, 2026

Ammonia → HCID 12272532, compound

https://huagongshe.com/reaction/1580157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
Reactant1-IndanoneHCID 6735—
ReactantSodium amideHCID 24533—
ReactantPhenyl 4-methylbenzoateHCID 219444—
SolventDiethyl EtherHCID 3283—
ProductHCID 12272532HCID 12272532—

Reaction Steps

To a suspension of 7.8 g. of sodium amide in 100 ml. anhydrous ether under an atmosphere of nitrogen is added 13.2 g. of indan-1-one. Ammonia is evolved and the mixture is stirred and heated under reflux until evolution ceases, after about 1 hour. A solution of 21.2 g. of phenyl p-toluate in 250 ml. of ether is then added dropwise over a period of 15 min. and the resulting mixture is heated under reflux for 11/2 hr. It is then cooled and poured onto 500 g. of ice, and then made slightly acidic by the addition of 2N hydrochloric acid. The organic layer is separated and washed twice with a 10% solution of sodium bicarbonate and once with water. It is then shaken with a saturated aqueous solution of cupric acetate, and the 2-phase system is stirred vigorously overnight. The resulting brown solid produced is filtered off and added to a stirred mixture of 250 ml. of ether and 100 ml of 2N hydrochloric acid. After 1 hr. the ether layer is separated, washed with sodium bicarbonate solution and water and dried over sodium sulfate. Removal of the ether gives a crude crystalline residue which can be recrystallized from ether to give the title product (m.p. 103°-105°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932430
Source datasetuspto-grants-1976_01
ORD IDord-c1e639f9c9a74bc7bc5e70094a69261b
Source noteuspto-grants-1976_01