HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771963Generated: October 31, 2026
HCID 90079870, compound → HCID 90080019, compound
https://huagongshe.com/reaction/1771963
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 90079870 | HCID 90079870 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 90080019 | HCID 90080019 | 100% |
Reaction Steps
To a solution of (2R,3S)-1-benzyl 4-tert-butyl 2,3-bis(cyclopropylmethyl)succinate, Intermediate S8G (0.530 g, 1.423 mmol) in MeOH (10 mL) was added 10% Pd/C (Degussa) (0.300 g, 1.423 mmol). The reaction mixture was evacuated with vacuum and filled with H2 (Repeated this for 3×). Next, the reaction mixture was stirred under H2 balloon for 1.5 h, evacuated, and filled with N2. The mixture was then filtered through CELITE®. The filtrate was concentrated to afford (2R,3S)-4-(tert-butoxy)-2,3-bis(cyclopropylmethyl)-4-oxobutanoic acid, Intermediate S8 (0.400 g, 1.417 mmol, 100% yield) as a colorless liquid. 1H NMR (400 MHz, chloroform-d) δ 2.69 (td, J=9.9, 3.7 Hz, 2H), 1.71-1.54 (m, 2H), 1.47 (s, 9H), 1.38-1.22 (m, 2H), 0.80-0.62 (m, 2H), 0.51-0.36 (m, 4H), 0.16-0.05 (m, 2H), 0.05-−0.02 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249157B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-00dce0db0cf24b7d912edfaa5c2c3567 |
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| Source note | uspto-grants-2016_02 |
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