HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711415Generated: November 3, 2026
Hydrochloric Acid → 4-[3-(1-Naphthylsulfonylmethyl)-4-nitrophenoxymethyl]piperidine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/1711415
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-((Chloromethyl)sulfonyl)naphthalene | HCID 11736608 | — |
| Reactant | 1-(Benzyloxycarbonyl)-4-[(4-nitrophenoxy)methyl]piperidine | HCID 19992422 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-(1-Naphthylsulfonylmethyl)-4-nitrophenoxymethyl]piperidine-1-carboxylic acid benzyl ester | HCID 58828632 | 74.1% |
Reaction Steps
A mixture of 4-(4-nitrophenoxymethyl)piperidine-1-carboxylic acid benzyl ester (0.8 g, 2.16 mmoles) and 1-chloromethanesulfonylnaphthalene (1.03 g, 4.3 mmoles) in THF (50 ml) at −78° C., under nitrogen, was treated dropwise with a solution of 1M potassium t-butoxide (6.5 ml, 6.5 mmoles) over a 30 minute period, allowed to warm to −40° C., stirred at −40° C. for 5 hours, poured into cold 2N HCl and extracted with EtOAc. The extracts were combined, dried over Na2SO4, and concentrated under vacuum. The resultant was purified by normal phase HPLC on a silica column, using as eluent 40% EtOAc/hexane, to afford the title compound as an off-white solid (0.9 g, 1.6 mmoles).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790751B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-9ea5f8607bad450da54c543cba6e9390 |
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| Source note | uspto-grants-2010_09 |
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