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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712459Generated: October 26, 2026

Formaldehyde → 6-Benzyl-1-methyloctahydropyrrolo[3,4-b]pyridine

https://huagongshe.com/reaction/712459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
Reactant6-Benzyloctahydro-1H-pyrrolo[3,4-b]pyridineHCID 11356376—
SolventFormic AcidHCID 284—
Product6-Benzyl-1-methyloctahydropyrrolo[3,4-b]pyridineHCID 1507000845%

Reaction Steps

A solution of 6-benzyloctahydro-1H-pyrrolo[3,4-b]pyridine (2.00 g) and 37% HCHO (6.0 mL) in HCO2H was heated to 90° C. and stirred for 4 h. The reaction mixture was cooled to rt and poured into ice-water. The mixture was adjusted to pH 10 with 2M NaOH aqueous solution and extracted with CH2Cl2 (70 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was chromatographed with a silica gel column (eluting agent: 20:1 (v/v) DCM/MeOH) to give the title compound as pale yellow oil (0.95 g, 45.00%), HPLC: 85.00%. The compound was characterized by the following spectroscopic data: MS (ESI, pos. ion) m/z: 231.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181277B2
Source datasetuspto-grants-2015_11
ORD IDord-28438f15f21d400c9a2537d9d40c9146
Source noteuspto-grants-2015_11