Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225047Generated: October 30, 2026

Ammonium Chloride → 3-Amino-5-(3-ethoxypropyl)-5H-dibenzo[a,d]cyclohepten-5-ol

https://huagongshe.com/reaction/225047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-bromo-3-ethoxypropaneHCID 260493—
ReactantMagnesiumHCID 5462224—
ReactantHCID 15628542HCID 15628542—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-5-(3-ethoxypropyl)-5H-dibenzo[a,d]cyclohepten-5-olHCID 23328876—

Reaction Steps

Magnesium turnings (6.2 g., 0.255 mole) covered with dry tetrahydrofuran (30 ml.) in carefully-dried apparatus are treated with a solution of 3-ethoxypropylbromide (42.5 g., 0.255 mole) added dropwise to maintain reflux. After preparation of the Grignard reagent according to standard procedures, the mixture is cooled, and 16 g. (0.072 mole) of 3-amino-5H-dibenzo[a,d]cyclohepten-5-one added in portions over 5 minutes. The reaction is stirred 15 minutes, then poured into 200 ml. of saturated aqueous ammonium chloride. The layers are separated, and the aqueous layer extracted once with ether. The ether layer, combined with the original organic phase, is washed once with water, dried over sodium sulfate, and evaporated in vacuo to give the title compound in essentially quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235820
Source datasetuspto-grants-1980_11
ORD IDord-872941dbf2144ede84b3f8f4f425ab9a
Source noteuspto-grants-1980_11