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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977163Generated: November 2, 2026

Acetic Anhydride → HCID 11100967, compound

https://huagongshe.com/reaction/977163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactantp-ToluenesulfonateHCID 85570—
ReactantHCID 11759565HCID 11759565—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 11100967HCID 1110096797%

Reaction Steps

3.4 ml (3.6×10-2 mole) of acetic anhydride was added to a solution of 8 g (2.4×10-2 mole) of 1-dodecyl-N,β,β-trimethyl-4-piperidineethanamine in 100 ml of dichloromethane and 16.8 ml of N,N-diethylethanamine. The reaction mixture was stirred for 12 hours at room temperature. The solution was poured into a 1N sodium hydroxide solution and extracted with trichloromethane. The organic phase was washed with water, dried and filtered and the solvents were evaporated off under reduced pressure. 8.7 g of N-methyl-N-[2-methyl-2-[(1-dodecyl)-4-piperidinyl]propyl]acetamide (yield: 97%) was obtained, from which the 4-methylbenzene sulphonate was prepared and recrystallised from ethyl acetate. M Pt=102°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614534
Source datasetuspto-grants-1997_03
ORD IDord-e04cc752d671495b92858cd4a5fff989
Source noteuspto-grants-1997_03