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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907177Generated: October 31, 2026

Acetyl chloride → 1-(6-Nitroindolin-1-yl)ethanone

https://huagongshe.com/reaction/907177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant6-NitroindolineHCID 29757—
SolventTetrahydrofuranHCID 8028—
Product1-(6-Nitroindolin-1-yl)ethanoneHCID 258566100.7%

Reaction Steps

6-Nitroindoline (3.0 g, 18.3 mmol) was dissolved in THF (45 mL) and Et3N (3.4 mL, 24.4 mmol) at 0° C. Acetyl chloride (1.5 mL, 21 mmol) was added dropwise. The mixture was stirred at room temperature for 30 minutes. The mixture was partitioned between EtOAc and aqueous HCl. The organic layer was dried and concentrated to yield 1-acetyl-6-nitroindoline (3.8 g, 100%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013006B2
Source datasetuspto-grants-2011_09
ORD IDord-3971a915551b4b56a3e6d6cfd651cbcd
Source noteuspto-grants-2011_09