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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912770Generated: November 2, 2026

Acetic Anhydride → HCID 59725957, compound

https://huagongshe.com/reaction/1912770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 23155162HCID 23155162—
SolventDichloromethaneHCID 6344—
ProductHCID 59725957HCID 59725957—

Reaction Steps

In 8 mL of methylene chloride, 387 mg (1.52 mmol) of 1-(4-nitrophenyl)-1H-indole-4-ol was dissolved, and 0.186 mL (2.00 mmol) of acetic anhydride and 0.318 mL (2.28 mmol) of triethylamine were added thereto and the mixture solution was stirred at room temperature for 14 hours. The reaction solution was partitioned between methylene chloride (50 mL) and a saturated ammonium chloride aqueous solution (20 mL) and washed with a saturated sodium chloride solution, and the organic layer was dried and then concentrated under reduced pressure to obtain acetic acid 1-(4-nitrophenyl)-1H-indol-4-yl ester. The product was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-45b97020bb0e4d08b93e179e170db6f6
Source noteuspto-grants-2013_12