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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420671Generated: November 1, 2026

Acetic Anhydride → HCID 54314519, compound

https://huagongshe.com/reaction/1420671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 53792914HCID 53792914—
SolventFormic AcidHCID 284—
ProductHCID 54314519HCID 54314519—

Reaction Steps

(S)-1-Indan-1-yl-4-phenylamino-piperidine-4-carbonitrile (27 mmol) was added dropwise at room temperature to a mixture of acetic anhydride and formic acid (40 ml each). The mixture was stirred for 16 h at room temperature. Sodium hydroxide solution was added (pH=7) and the mixture extracted with ethyl acetate. Organic phases were pooled, dried with sodium sulfate and concentrated. Chromatography on silica gel (ethyl acetate) yielded the formulated amine which was dissolved in t-butanol (60 ml). Ammonia (28%, 10 ml), water (10 ml) and hydrogen peroxide solution (33% in water, 5 ml) were added. The mixture was stirred for 2.5 h at room temperature (RT, about 22° C.), quenched with cold water (50 ml) and extracted with methylene chloride. Organic phases were pooled, dried with sodium sulfate and concentrated. Chromatography on silica gel (methylene chloride/methanol, 98:2) yielded the desired product as a solid. 1.0 g (11%) of (S)-1-indan-1-yl-4-phenylamino-piperidine-4-carboxylic acid amide, m.p. 194-195° C. and MS: m/e=336.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071925
Source datasetuspto-grants-2000_06
ORD IDord-1a319687dae94e90911397c82b84a3c8
Source noteuspto-grants-2000_06