HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778510Generated: November 4, 2026
Benzyl chloroformate → HCID 117697513, compound
https://huagongshe.com/reaction/1778510
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 3-Oxa-9-azabicyclo[3.3.1]nonan-7-one--hydrogen chloride (1/1) | HCID 71627138 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 117697513 | HCID 117697513 | 65.2% |
Reaction Steps
3-oxa-9-azabicyclo[3.3.1]nonan-7-one hydrochloride (CAS 1126795-00-3) (10 g) was dissolved in 200 ml of dichloromethane which was cooled to 0° C. Then, CbzCl (14.3 g, 84.7 mmol) was added to the mixture followed by the dropwise addition of a solution of TEA (14.6 ml, 112.8 mmol) in 20 ml of dichloromethane. The mixture was allowed to warm up to room temperature. After stirring 2 h, it was quenched with 20 ml of a saturated aqueous solution of NaHCO3. The two layers were separated and the aqueous layer was extracted with dichloromethane (3×150 ml). The combined organic layers were washed with water, dried over Na2SO4 and the solvent was evaporated under reduced pressure. The crude product was purified by chromatography on silica gel, yielding 10.1 g of benzyl 7-oxo-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate 100b (64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266904B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-21761757798f44a291b1aaf2187accea |
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| Source note | uspto-grants-2016_02 |
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