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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422243Generated: October 29, 2026

3-Methylbutanal → HCID 11199441, compound

https://huagongshe.com/reaction/422243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethylbutanalHCID 11552—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59750673HCID 59750673—
SolventMethanolHCID 887—
ProductHCID 11199441HCID 1119944166.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101638B2
Source datasetuspto-grants-2012_01
ORD IDord-5dbcd585efe4462b9f3d5257236298c4
Source noteuspto-grants-2012_01