Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372027Generated: October 30, 2026

Acetic Anhydride → HCID 15678881, compound

https://huagongshe.com/reaction/2372027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15678877HCID 15678877—
SolventDichloromethaneHCID 6344—
ProductHCID 15678881HCID 1567888131.8%

Reaction Steps

A catalytic amount, (0.019 g) of N,N-dimethylaminopyridine was added to a deoxygenated solution of 5.8 g of 1,2,3,4,5,6-hexahydro-1,3-dimethyl-2,6-methano-1,3-benzodiazocin-8-ol and 5.4 g of acetic anhydride in 270 ml of dichloromethane. After stirring for 15 minutes, the reaction mixture was treated with a saturated sodium bicarbonate solution. The aqueous layer was separated and extracted with dichloromethane. The combined organic layers were washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated to an oil (7.1 g). Column chloromatography of a 3.5 g aliquot of the oil (silica gel; elution with triethylamine-methanol-ethyl acetate) afforded 2.2 g of 1,2,3,4,5,6-hexahydro-1,3-dimethyl-2,6-methano-1,3-benzodiazocin-8-ol acetate as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05097033
Source datasetuspto-grants-1992_03
ORD IDord-15a64fb5789043f5b49516336653d859
Source noteuspto-grants-1992_03