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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870342Generated: October 30, 2026

Acetic Anhydride → HCID 22145880, compound

https://huagongshe.com/reaction/1870342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 22145850HCID 22145850—
SolventWaterHCID 962—
ProductHCID 22145880HCID 22145880—

Reaction Steps

Acetic anhydride (10 mL) is treated with N-(2,6-dichloro-4-aminophenyl)-3-cyclopentyloxy-4-methoxybenzamide (0.8 g; that is prepared as described in Example 11), and the reaction mixture is stirred for 2 hours and left to stand overnight. It is then poured into water (100 mL), and extracted with ethyl acetate (100 mL) and then with dichloromethane (100 mL). The organic extracts are combined, dried over magnesium sulfate, and evaporated, to give N-(4-acetylamino-2,6-dichlorophenyl)-3-cyclopentyloxy-4-methoxybenzamide (0.4 g), m.p. 250-252° C. [Elemental analysis: C,57.6; H,5.05; N,6.3; Cl,6.1%; calculated: C,57.5; H,5.1; N,6.4; Cl, 16.2%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096768
Source datasetuspto-grants-2000_08
ORD IDord-2beaafae8e5045d4b263f8d89583b976
Source noteuspto-grants-2000_08