HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351751Generated: November 4, 2026
HCID 11522987, compound → HCID 86591983, compound
https://huagongshe.com/reaction/1351751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11522987 | HCID 11522987 | — |
| Reactant | HCID 20070078 | HCID 20070078 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86591983 | HCID 86591983 | 96% |
Reaction Steps
To a solution of (5-cyano-7-hydroxymethyl-8-methyl-1-propyl-1,3,4,9-tetrahydro-pyrano[3,4-b]indol-1-yl)-acetic acid (8.28 g, 22 mmol) in dichloroethane/benzene (85 mL/85 mL) was added a homogeneous mixture of activated MnO2 (19.4 g, 223 mmol) and Celite (19.4 g). The solution was heated to 40° C. and agitated vigorously for 1.3 hours. The reaction was cooled, diluted with EtOAc and filtered through Celite. Concentration of the filtrate in vacuo afforded 7.88 g (96%) of a pale yellow foam. 1H NMR (CDCl3) δ 10.31 (bs, 1 H), 10.27 (s, 1H), 7.90 (s, 1H), 4.27 (m, 2H), 4.11 (m, 1H), 3.95 (m, 1H), 3.09 (m, 2H), 3.04 (d, J=17.0 Hz, 1H), 2.95 (d, J=7.6 Hz, 1H), 2.57 (s, 3H), 2.00 (m, 2H), 1.30 (m, 4H), 0.90 (t, J=7.62 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217730B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-370f3e394bda4d0481ef00623eacff91 |
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| Source note | uspto-grants-2007_05 |
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