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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762322Generated: November 1, 2026

Propionic anhydride → HCID 178460016, compound

https://huagongshe.com/reaction/1762322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic anhydrideHCID 31263—
ReactantHCID 178420312HCID 178420312—
ProductHCID 178460016HCID 178460016—

Reaction Steps

A 250 ml r.b. flask was charged with 1-benzyl-4-(1H-tetrazol-5-yl)-4-anilinopiperidine (17.7 g, 53 mmol) and propionic anhydride (95 ml). The resulting mixture was stirred at 70°-75° C. for 6 hours. Then, it was concentrated in vacuo and the crude was chromatographed (SiO2, 5-20% MeOH/CH2Cl2) to give the desired compound (14.7 g, 32 mmol) as white powder: m.p. 226-228 C; R (nujol) 1660 cm-1 ; MR (270 MHz, CDCl3) δ0.864, (t, 3H, CH3CH2CON), 1.175 (t, 3H, CH3CH2CO2H), 1.883 (q, 2H, CH3CH2CO2H), 2.113 (m, 4H), 2.395 (q, 2H, CH3CH2CO2H), 2.8-3.1 (m, 4H), 3.464 (s, 2H, benzyl CH2), 7.1 to 7.5 (complex, 10H, phenyl H's). Anal. Calcd. for C22H26N6O. C3H6O2 : C,64.64; H,6.94; N,18.09. Found: C, 64.65; H, 7.00; N, 17.89. ##STR22##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831192
Source datasetuspto-grants-1989_05
ORD IDord-ba5caa83fb4c43848328b927b5c3bae4
Source noteuspto-grants-1989_05