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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554476Generated: October 29, 2026

Acetic Acid → 9-(3,4-Dichloro-phenylamino)-3-aza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/554476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3,4-DichloroanilineHCID 7257—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylateHCID 51072194—
Solvent1,2-DichloroethaneHCID 11—
Product9-(3,4-Dichloro-phenylamino)-3-aza-spiro[5.5]undecane-3-carboxylic acid tert-butyl esterHCID 6745921830%

Reaction Steps

3,4-Dichloroaniline (364 mg, 2.2 mmol), sodium triacetoxyborohydride (889 mg, 4.20 mmol) and acetic acid (0.24 mL, 4.20 mmol) were added to a solution of 9-oxo-3-aza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester (561 mg, 2.10 mmol) in 1,2-dichloroethane (30 mL) with crunched 4A mol sieves (10 g). The mixture was stirred a room temperature over night. Additional 4A mol sieves (12 g) and sodium triacetoxyborohydride (445 mg) was added and the mixture was stirred over night. The reaction was quenched with water and 5% citric acid was added. The mixture was filtered through kieselguhr and the filtrated was evaporated until only the aqueous layer remained. The aqueous layer was extracted with ethyl acetate (3×50 mL) and the combined organic phases were washed with brine, dried with sodium sulphate, filtered and evaporated to give the crude product. Flash chromatography (ethyl acetale/heptane) gave 9-(3,4-dichloro-phenylamino)-3-aza-spiro[5.5]undecane-3-carboxylic acid tert-butyl ester (258 mg, 0.624 mmol, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049012B2
Source datasetuspto-grants-2011_11
ORD IDord-7c95454c58b8494da1dadab1be3a1192
Source noteuspto-grants-2011_11