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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350Generated: October 27, 2026

Hexamethyldisilazane → 1-(3-Indanyloxy-4-methoxyphenyl)propylamine

https://huagongshe.com/reaction/2350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Indanyloxy-4-methoxybenzaldehydeHCID 57257970—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418443HCID 178418443—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-(3-Indanyloxy-4-methoxyphenyl)propylamineHCID 570150489%

Reaction Steps

To an ice bath cooled stirred solution of 1,1,1,3,3,3-hexamethyldisilazane (2.7 mL, 13 mmol) in tetrahydrofuran (5 mL) under nitrogen, was added a hexane solution of butyl lithium (2.5M, 4.8 mL, 12 mmol) via syringe. The ice bath was removed and the solution was stirred for 25 minutes at room temperature. This solution then was added dropwise to an ice bath cooled solution of 3-indanyloxy-4-methoxybenzaldehyde (2.68 g, 10.0 mmol) in tetrahydrofuran (4 mL) and the mixture was stirred for one hour. An ethereal solution of ethylmagnesium bromide (3M, 6.7 mL, 20 mmol) then was added dropwise via syringe. The reaction mixture was heated at reflux and was monitored by HPLC (Waters Nova-Pak/EC 18 column, 3.9×150 mm, 4 micron, 1 mL/min, 240 nm, 40/60, CH3CN/0.1% H3PO4 (aq)). After 48 hours the reaction had reached completion and was allowed to cool to room temperature. The reaction mixture then was slowly poured into a saturated solution of ammonium chloride (80 mL). The resulting mixture was extracted with methylene chloride (3×15 mL) and the combined extracts were dried over magnesium sulfate and concentrated to afford the product which was further purified by flash column chromatography (silica gel, 250/10/1, methylene chloride/methanol/ammonium hydroxide) to afford 0.27 g (9%) of product as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728844
Source datasetuspto-grants-1998_03
ORD IDord-a172f4e4b1614e5bac954c6d01d97ff6
Source noteuspto-grants-1998_03