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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257529Generated: October 27, 2026

Triethylamine → Tert-butyl 3-bromo-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)benzoate

https://huagongshe.com/reaction/1257529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethylenecyclobutaneHCID 14262—
ReactantChlorosuccinimideHCID 31398—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl 3-bromo-5-[(E)-hydroxyiminomethyl]benzoateHCID 58096166—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 3-bromo-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)benzoateHCID 5809613844.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl 3-bromo-5-[(E)-(hydroxyimino)methyl]benzoate (5.26 g, 17.5 mmol) in N,N-dimethylformamide (80 mL)) was added N-chlorosuccinimide (2.57 g, 19.3 mmol). The reaction mixture was heated to 50° C. After 1 h, the reaction was cooled to ambient temperature and methylenecyclobutane (6.49 mL, 70.1 mmol) was added. Triethylamine (12.2 mL, 88.0 mol) was added. The mixture was stirred at ambient temperature. After 10 min, saturated aqueous NaHCO3 was added and the mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with water (2×), brine, dried over sodium sulfate, filtered and concentrated. Purification by silica gel chromatography (100% hexanes→90% hexanes/ethyl acetate) gave the title compound (2.86 g). MS 366 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461185B2
Source datasetuspto-grants-2013_06
ORD IDord-2748f007a4b2492e92b261c7007d960b
Source noteuspto-grants-2013_06