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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947501Generated: October 27, 2026

Acetic Anhydride → Tert-butyl 9-acetyl-3,9-diazaspiro[5.5]undecane-3-carboxylate

https://huagongshe.com/reaction/1947501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 15296367—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 9-acetyl-3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 66786450100.1%

Reaction Steps

To a solution of 3,9-diaza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester (400 mg, 1.57 mmol) in DCM (16 mL) was added acetic anhydride (177 μL, 1.88 mmol) and triethylamine (656 μL, 4.71 mmol) and the mixture was stirred (rt, 16 h). The reaction mixture was diluted with DCM (16 mL), washed with water (3×10 mL) and brine (1×10 mL). The organic layer was dried, filtered and concentrated in vacuo to provide the 9-acetyl-3,9-diaza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester (466 mg, 100%). This intermediate was dissolved in DCM (4 mL), treated with HCl (4 M in dioxane, 4 mL) and stirred (rt, 16 h). The dispersion was concentrated in vacuo to provide the title compound as a white powder (365 mg, 100%). MS (ESI): mass calcd. for C11H20N2O, 196.16; m/z found, 197.1 [M+H]+. 1H NMR (400 MHz, MeOD): 3.63-3.51 (m, 4H), 3.23-3.17 (m, 4H), 2.13 (s, 3H), 1.82-1.73 (m, 4H), 1.67-1.53 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399465B2
Source datasetuspto-grants-2013_03
ORD IDord-76769a6e9ad3434b98bb278b4eb576c9
Source noteuspto-grants-2013_03