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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863492Generated: October 30, 2026

Acetic Anhydride → N-(5-acetylamino-indan-2-yl)-acetamide

https://huagongshe.com/reaction/863492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantN-(5-nitro-indan-2-yl)-acetamideHCID 14820512—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-acetylamino-indan-2-yl)-acetamideHCID 1969625452%

Reaction Steps

The mixture of N-(5-nitro-indan-2-yl)-acetamide (20.5 g, 93 mmol) in tetrahydrofuran (200 mL) was combined with acetic anhydride (10 mL) and Raney nickel (5 g) and stirred under an atmosphere of hydrogen gas (in a balloon) at room temperature for 24 h. Additional Raney nickel was added and the balloon recharged with hydrogen gas and stirred an additional 24 h. After removing the Raney nickel by filtration through a celite pad and washing with methanol several times, the filtrate was evaporated to a syrup. The residue was triturated with ether/water and the resulting white solid collected by filtration (9.2 g, 52% yield overall from 2-aminoindan, prepared in Example 20).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721234
Source datasetuspto-grants-1998_02
ORD IDord-c15d85db7cec434a938c1f42cc3374b4
Source noteuspto-grants-1998_02