HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044334Generated: October 31, 2026
Benzene → Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride
https://huagongshe.com/reaction/1044334
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-Benzocyclobutenecarboxylic acid | HCID 302324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride | HCID 22956883 | — |
Reaction Steps
Thionyl chloride (0.5 ml) was added to a solution of bicyclo[4.2.0]octa-1,3,5-triene-7-carboxylic acid [14381-41-0] (0.001 mol) in dichloromethane. The reaction mixture was refluxed for 1 hour. Then stirred overnight at room temperature. The solvents were co-evaporated 2 times with benzene to obtain bicyclo[4.2.0]octa-1,3,5-triene-7-carbonyl chloride [1473-47-8] which was dissolved in DIPE. The obtained solution was added dropwise to a cooled mixture (0° C.) of N-allyl-2-adamantanamine [24161-63-5] and sodium carbonate in DIPE. The reaction mixture was stirred for 30 minutes on ice and then for 2 hours at room temperature. The mixture was poured out into water and extracted with dichloromethane. The organic layer was filtered through Extrelut™ and the filtrate was evaporated. The residue was purified by flash column chromatography on TRIKONEX FlashTube™ (eluent: CH2Cl2/EtOAc 90/10). The product fractions were collected and the solvents were evaporated, yielding 0.13 g of intermediate 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563591B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-a9d157de15354e29bf7625bcbaa202ed |
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| Source note | uspto-grants-2013_10 |
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