HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664600Generated: October 27, 2026
Benzyl chloroformate → 1,2-Dibenzyl 3-(tert-butyl) (2S,3S)-5-methylenepiperidine-1,2,3-tricarboxylate
https://huagongshe.com/reaction/1664600
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 2-Benzyl 3-(tert-butyl) (2S,3S)-1-benzyl-5-methylenepiperidine-2,3-dicarboxylate | HCID 16069575 | — |
| Product | 1,2-Dibenzyl 3-(tert-butyl) (2S,3S)-5-methylenepiperidine-1,2,3-tricarboxylate | HCID 16108937 | — |
Reaction Steps
A mixture of 2-benzyl 3-tert-butyl (2S,3S)-1-benzyl-5-methylenepiperidine-2,3-dicarboxylate from step 1d (2.3 g) and benzyl chloroformate (3 mL) was stirred at 65° C. for 28 h. The excess of the benzyl chloroformate was removed under reduced pressure. The residue was purified through Combiflash (hexane and ethyl acetate: gradient 0 to 10% during 12 min) to give the desired compound 1,2-dibenzyl 3-tert-butyl (2S,3S)-5-methylenepiperidine-1,2,3-tricarboxylate (1.40 g). MS (ESI): 488.1 (M+Na+); 366.1 (M+H+—COO(t-Bu)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039471B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-792c07e415d74411b049d4aed76aed08 |
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| Source note | uspto-grants-2011_10 |
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