Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089012Generated: October 30, 2026

Hydrochloric Acid → 5,6-Bis(acetoxy)-1-aminomethyl-3-phenyl-3,4-dihydronaphthalene hydrochloride

https://huagongshe.com/reaction/1089012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 19961108HCID 19961108—
Product5,6-Bis(acetoxy)-1-aminomethyl-3-phenyl-3,4-dihydronaphthalene hydrochlorideHCID 1996108429%

Reaction Steps

A suspension of 7.6 g (25 mmol) of 1-aminomethyl-3,4-dihydro-5,6-dihydroxy-3-phenyl-naphthalene hydrochloride (Example 2B) in 400 mL of acetic anhydride saturated with anhydrous hydrogen chloride was stirred at ambient temperature for 48 h. Diethyl ether (approximately 2 L) was added and a solid was collected by filtration and washed with diethyl ether. Crystallization of the crude material (6.7 q) was achieved by dissolving the powder in 400 mL of hot ethanol, adding 100 mL of water, filtering the solution hot and allowing it to cool. The white crystals which formed were filtered and dried to give 2.8 g (29% yield) of 1-aminomethyl-5,6-bis(acetoxy)-3,4-dihydro-3-phenyl-naphthalene hydrochloride, m.p. 207°-208° C. 1H NMR (d6DMSO) delta 2.28 (s, 6H), 2.62 (dd, 1H), 2.95 (dd, 1H), 3.7-3.8 (m, 1H), 3.97 (s, 2H), 6.25 (d, 1H), 7.19 (d, 1H), 7.2-7.4 (m, 6H), 8.41 (br s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963568
Source datasetuspto-grants-1990_10
ORD IDord-058203e6ba7f4c8a8ace85c04d5e8ea6
Source noteuspto-grants-1990_10