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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674725Generated: October 31, 2026

Methanol → HCID 16730115, compound

https://huagongshe.com/reaction/1674725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3,3-DimethylbutanalHCID 76335—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58966608HCID 58966608—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 16730115HCID 16730115—

Reaction Steps

A solution of 3,3-dimethylbutyraldehyde (13 mg, 0.13 mmol) and the spiro-piperidine (B5) (25 mg, 0.10 mmol) in dry dichloromethane (2 ml) was stirred at room temperature for 30 min, cooled with ice-bath, and treated with sodium triacetoxyborohydride (44 mg, 0.2 mml), followed by acetic acid (1 drop) and methanol (1 ml). The reaction mixture was stirred for another 5 hours and concentrated under a stream of nitrogen. The residue was dissolved in methanol (1 ml) and purified by reverse phase HPLC to give the title compound no. 17 as a TFA salt. LC-MS: m/e=343.30 (M+H). Rt=1.63 min. 1H-NMR (500 MHz, DMSO-d6): 9.28 (br.s, 1H), 8.18 (d, 1H), 7.35 (d, 1H), 7.30 (t, 1H), 7.19 (t, 1H), 7.16 (d, 1H), 4.92 (m, 1H), 3.45 (m, 2H), 3.14 (m, 4H), 2.19 (m, 2H), 2.05 (m, 1H), 1.87 (s, 3H), 1.82 (m, 2H), 1.73 (d, 1H), 1.60 (m, 3H), 0.93 (m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003660B2
Source datasetuspto-grants-2011_08
ORD IDord-bef05cc631054949995534908501d473
Source noteuspto-grants-2011_08