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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489675Generated: November 2, 2026

Acetic Anhydride → HCID 22145880, compound

https://huagongshe.com/reaction/1489675

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,16.1%; calculated: C,57.5; H,5.1; N,6.4; Cl,16.2%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679696
Source datasetuspto-grants-1997_10
ORD IDord-abddce9e6f4f4fac98aa999549624400
Source noteuspto-grants-1997_10