HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422243Generated: October 29, 2026
3-Methylbutanal → HCID 11199441, compound
https://huagongshe.com/reaction/422243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methylbutanal | HCID 11552 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59750673 | HCID 59750673 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11199441 | HCID 11199441 | 66.9% |
Reaction Steps
Add isovaleraldehyde (64.5 mg, 0.750 mmol) to a solution of 6-(5-aminomethyl-5,6,7,8-tetrahydro-naphthalen-2-yloxy)-nicotinamide (intermediate 21, 148 mg, 0.500 mmol) dissolved in MeOH (5 mL) and stir at ambient temperature for 1.5 hours before adding NaBH4 (38 mg, 1.00 mmol). After stirring for an additional two hours, concentrate the reaction mixture and redissolved in EtOAc. Wash the EtOAc solution with 5% aq. KOH and brine before drying (MgSO4) and concentrating. Purify on silica gel (5% (1N NH3/MeOH)/DCM) to obtain 123 mg of the title compound as a white foam. Mass spectrum (ion spray): m/z=368 (M+1); 1HNMR (CDCl3): 8.59 (s, 1H), 8.15 (d, 1H), 7.25 (d, 1H), 6.94 (d, 1H), 6.89 (d, 1H), 6.85 (s, 1H), 5.82 (br. s, 2H), 2.97 (m, 1H), 2.84 (m, 2H), 2.76 (m, 2H), 2.66 (m, 2H), 1.85 (m, 3H), 1.74 (m 1H), 1.62 (m, 1H), 1.41 (m, 2H), 0.90 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101638B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-5dbcd585efe4462b9f3d5257236298c4 |
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| Source note | uspto-grants-2012_01 |
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