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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357391Generated: November 3, 2026

Benzoyl chloride, 3-nitro- → HCID 18506156, compound

https://huagongshe.com/reaction/1357391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantHCID 18506136HCID 18506136—
SolventAcetoneHCID 180—
ProductHCID 18506156HCID 18506156—

Reaction Steps

2-[3,4-Bis-(1-benzyl-1H-tetrazol-5-yl)phenoxy]phenylamine (37 mg, 0.07 mmol) and TEA (19 mg, 0.18 mmol) were mixed in acetone (10 ml), and 3-nitrobenzoyl chloride (15 mg, 0.08 mmol) was added. The reaction mixture was stirred for 120 hours at room temperature. The reaction mixture was evaporated in vacuo to an oil. The oil was purified on a silica column with methylene chloride/methanol (39:1) as eluent. The title compound was isolated as yellow oil (yield: 30 mg (62%). 1H-NMR (CDCl3 in ppm): 5.6 (4H,2xs); 7.0 (1H,d,d); 7.15 (1H,d,d); 7.2 (1H,d,d); 7.25-7.4 (11H,m); 7.6 (1H,d,d); 7.73 (1H,d); 7.9 (1H,d); 8.1 (1H,d,d); 8.35 (1H,d,d); 8.45 (1H,broad s); 8.55 (1H,d,d); 8.7 (1H,d,d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06590118B1
Source datasetuspto-grants-2003_07
ORD IDord-0027b81ff3764a21913fd50c5502472c
Source noteuspto-grants-2003_07