HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72126Generated: October 27, 2026
Hydrochloric Acid → 2-Adamantyl 3-((tert-butoxycarbonylamino)methyl)azetidine-1-carboxylate
https://huagongshe.com/reaction/72126
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-adamantyl Chloroformate | HCID 10878537 | — |
| Reactant | tert-butyl N-(azetidin-3-ylmethyl)carbamate | HCID 15346872 | — |
| Product | 2-Adamantyl 3-((tert-butoxycarbonylamino)methyl)azetidine-1-carboxylate | HCID 44473366 | 23% |
Reaction Steps
A vial was charged with tert-butyl azetidin-3-ylmethylcarbamate (25 mg, 0.12 mmol), i-Pr2NEt (31 μL, 0.17 mmol) and a flea stir bar. A solution of 2-adamantyl chloroformate in CH2Cl2 (1.5 mL, 17 mg mL−1, 0.12 mmol) was added. The mixture was stirred overnight at rt. A 10-mL ChemElut cartridge (Varian Inc. catalog number 12198007) was wetted with 5% aq HCl (5 mL) and allowed to stand for 5 min. The reaction mixture was applied to the cartridge and eluted with ether (20 mL). The eluate was evaporated to dryness and the residue was purified by preparative HPLC to afford the title compound (10 mg, 23%). 1H NMR (CDCl3) δ 1.42 (s, 9H), 1.5-2.0 (14H), 2.76 (m, 1H), 3.35 (m, 2H), 3.67 (m, 2H), 4.03 (m, 2H), 4.68 (m, 1H), 4.78 (s, 1H); LC-MS Method 1 tR=2.08 min, m/z=387, 365, 309.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828985B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2d93cf5715574d9f865ec399ec289624 |
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| Source note | uspto-grants-2014_09 |
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