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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176342Generated: October 29, 2026

Aniline → Isobutyranilide

https://huagongshe.com/reaction/2176342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
SolventTetrahydrofuranHCID 8028—
ProductIsobutyranilideHCID 2043691%

Reaction Steps

First, 26.2 g of aniline, 100 mL of tetrahydrofuran (THF), and 56.9 g of triethylamine (Et3N) were put in a 500 mL three-neck flask, and mixed. Then, under cooling in ice, a mixed solution of 30 g of isobutyryl chloride and 100 mL of THF was dripped through a 50 mL dropping funnel to the above mixed solution, and then the temperature was increased to room temperature and the solution was stirred for 19 hours to be reacted. After the reaction, this mixture was subjected to suction filtration to give a filtrate. The resulting filtrate was washed with water, and then saturated saline, and anhydrate magnesium sulfate was added for drying. After the drying, the mixture was subjected to gravity filtration, and the filtrate was concentrated, so that N-phenylisobutyramide was prepared (a white solid, yield: 91%). The synthetic scheme of Step 1 is shown by (a-10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09065061B2
Source datasetuspto-grants-2015_06
ORD IDord-c2e6a5ed43ba4ce29c32ee684f483df9
Source noteuspto-grants-2015_06