HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922641Generated: October 30, 2026
HCID 59605965, compound → HCID 59605642, compound
https://huagongshe.com/reaction/1922641
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 59605965 | HCID 59605965 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 59605642 | HCID 59605642 | 92.2% |
Reaction Steps
A mixture of 3-(3,6-dihydro-2H-pyran-4-yl)azetidine-1-carboxylic acid tert-butyl ester (28.6 g, 0.12 mol) and 10% palladium on charcoal (5.0 g) in IMS (500 mL) was stirred under hydrogen (4 bar) at room temperature for 36 hours. The reaction mixture was filtered through a bed of Celite® which was washed with IMS. The filtrates were combined and concentrated to give a residue which was reacted as above for 18 hours. The reaction mixture was worked up as above to give a residue which was dried under reduced pressure to give 3-(Tetrahydropyran-4-yl)azetidine-1-carboxylic acid tert-butyl ester as a beige solid (26.7 g, 92%). 1H NMR (300 MHz, CHCl-d): δ 4.03-3.90 (m, 4H); 3.63 (dd, J=8.6, 5.7 Hz, 2H); 3.37 (td, J=11.8, 2.0 Hz, 2H); 2.32-2.19 (m, 1H); 1.63-1.48 (m, 3H); 1.44 (s, 9H); 1.29-1.12 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173650B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-f80476cf451b4a5f913be244e477898c |
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| Source note | uspto-grants-2012_05 |
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