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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187406Generated: October 31, 2026

Acetyl chloride → HCID 54490053, compound

https://huagongshe.com/reaction/2187406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantChloroform methanolHCID 21584188—
Reactant(R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthaleneHCID 53960413—
SolventDichloromethaneHCID 6344—
ProductHCID 54490053HCID 5449005393.4%

Reaction Steps

To an ice-cooled solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (100 mg, 0.41 mmol) and triethylamine (110 μL, 0.82 mmol) in methylene chloride (25 mL) was added acetyl chloride (31 μL, 0.43 mmol) in methylene chloride (10 mL). After the addition the reaction was allowed to reach room temperature and then washed with water. The phases were separated, the combined organic phases were dried (Na2SO4), filtered and evaporated in vacuo to give a crude product which was purified on a silica get column using chloroform/methanol/concentrated ammonium hydroxide (95:4:0.5) as the eluent. Yield: 110 mg (90%) of the title compound as an oil. Crystallization from ethyl acetate/hexane gave 52 mg (44% yield) of white crystals: mp 152-154° C.; [α]21D +66° (c 0.13, chloroform); EIMS (70 eV) m/z (relative intensity) 287 (9, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410530B1
Source datasetuspto-grants-2002_06
ORD IDord-6591a6046b76493abb1f345a8ffefb7a
Source noteuspto-grants-2002_06