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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methylenecyclobutane | HCID 14262 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-butyl 3-bromo-5-[(E)-hydroxyiminomethyl]benzoate | HCID 58096166 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 3-bromo-5-(5-oxa-6-azaspiro[3.4]oct-6-en-7-yl)benzoate | HCID 58096138 | 44.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461185B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-2748f007a4b2492e92b261c7007d960b |
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| Source note | uspto-grants-2013_06 |
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