Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662283Generated: October 29, 2026

Triethylamine → N-(1,3-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-3,3-dimethylbutanamide

https://huagongshe.com/reaction/1662283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
Reactant6-Amino-5,7-dimethyl-3,4-dihydronaphthalen-1(2H)-oneHCID 55271663—
SolventDichloromethaneHCID 6344—
ProductN-(1,3-dimethyl-5-oxo-5,6,7,8-tetrahydronaphthalen-2-yl)-3,3-dimethylbutanamideHCID 5980890492%

Reaction Steps

To a solution of 6-amino-5,7-dimethyl-3,4-dihydronaphthalen-1(2H)-one (1 g, 5.3 mmol) and triethylamine (1.07 g, 10.6 mmol) in anhydrous dichloromethane (20 ml) was added dropwise tert-butylacetyl chloride (0.78 g, 5.8 mmol) at room temperature. The reaction mixture was stirred an additional 3 hours at this temperature. The solvent was removed under reduced pressure, and the residue was purified by Biotage (hexane/EtOAc, 0-40%, 40 min) to give a white solid (1.4 g, 92%). 1H-NMR δ (CDCl3, 300 MHz): 7.82 (s, 1H), 6.73 (brs, 1H, exchangeable with D2O), 2.85 (t, J=6.0 Hz, 2H), 2.60 (t, J=6.0 Hz, 2H), 2.33 (s, 2H), 2.27 (s, 3H), 2.18 (s, 3H), 2.15 (m, J=6.0 Hz, 2H), 1.16 (s, 9H). MS: 288 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030518B2
Source datasetuspto-grants-2011_10
ORD IDord-d6d60b2894454ec09be266adfa0048c0
Source noteuspto-grants-2011_10