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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393206Generated: October 29, 2026

Propanal → HCID 11362947, compound

https://huagongshe.com/reaction/393206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanalHCID 527—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(7-Bromo-1,2,3,4-tetrahydro-naphthalen-2-ylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 11441209—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 11362947HCID 1136294786.7%

Reaction Steps

To a solution of 4-(7-bromo-1,2,3,4-tetrahydro-naphthalen-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester (610 mg, 1.5 mmol) and propionaldehyde (0.1 mL, 1.5 mmol) in dichloroethane (20 mL) under a nitrogen atmosphere was added sodium triacetoxyborohydride (795 mg, 3.75 mmol) in a single portion. The reaction was stirred at room temperature for 24 h then concentrated in vacuo. The residue was partitioned between EtOAc (75 mL) and 5% aq. KOH (50 mL). The aqueous phase was extracted twice more with EtOAc (2×30 mL). The combined organic layers were dried over MgSO4, filtered, and concentrated onto silica (10 g). This was placed on top of a flash column and eluted with 20% hexanes in acetone. The fractions containing product were pooled and concentrated to afford 4-[(7-bromo-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-piperidine-1-carboxylic acid tert-butyl ester (587 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806278B2
Source datasetuspto-grants-2004_10
ORD IDord-d0f72e9ca1564a249793e453102ad14c
Source noteuspto-grants-2004_10