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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356892Generated: October 30, 2026

Acetic Anhydride → HCID 22145880, compound

https://huagongshe.com/reaction/356892

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 numberUS05840724
Source datasetuspto-grants-1998_11
ORD IDord-d95311c23a274ff08cb54f3e384bee3b
Source noteuspto-grants-1998_11