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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742341Generated: October 31, 2026

Hydrochloric Acid → HCID 23365875, compound

https://huagongshe.com/reaction/1742341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium hydrideHCID 24758—
Reactant3-Methoxy-4-(5-nitroindol-3-ylmethyl)benzoic acidHCID 10269207—
SolventDimethylformamideHCID 6228—
ProductHCID 23365875HCID 2336587567.4%

Reaction Steps

A solution of 4-(5-nitroindol-3-ylmethyl)-3-methoxybenzoic acid (0.6 g.) in N,N-dimethylformamide (DMF), (3 ml.) was added to a stirred suspension of oil-free sodium hydride (0.088 g.) in DMF (8 ml.) under a nitrogen atmosphere at ambient temperature. The red solution was stirred for 20 minutes, and acetic anhydride (0.187 g.) added. After 1 hour, the mixture was poured into hydrochloric acid (1N, 30 ml.), extracted with ethyl acetate (3×50 ml), the combined extracts washed with water (2×20 ml.), brine, dried (MgSO4) and evaporated. The product was crystallized from a mixture of tetrahydrofuran and ether to give 4-(1-acetyl-5-nitroindol-3-ylmethyl)-3-methoxybenzoic acid (0.455 g., 67%) as a yellow powder; partial NMR (250 MHz, DMSO--d6): 2.68(s,3H, NCOCH3); 3.95(s,3H, OMe); 4.13(s,2H, ArCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338734
Source datasetuspto-grants-1994_08
ORD IDord-7d92ff9ff169452f8daa526d0e2b46fe
Source noteuspto-grants-1994_08