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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289475Generated: October 31, 2026

Sodium triacetoxyborohydride → 1-(Methoxymethyl)-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1289475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 12415172HCID 12415172—
SolventMethanolHCID 887—
Product1-(Methoxymethyl)-1,2,3,4-tetrahydroisoquinolineHCID 18315752—

Reaction Steps

Sodium triacetoxyborohydride (8.11 g, 38.3 mmol) was added to a stirred, ice-cooled solution of the product from (b) above (6.1 g, 34.8 inmol) in methanol (80 ml), then the resulting mixture stirred for 18 hours at room temperature before being quenched with water. The bulk of the solvent was removed under reduced pressure, then the residue basified with 1M aqueous sodium hydroxide solution and extracted with dichloromethane. The extract was washed with saturated brine, dried (MgSO4) and evaporated under reduced pressure to furnish the required product (6.19 g) as an orange oil, Rf 0.25 (SS 3), m/e 178 (M+H)+, which was used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750520
Source datasetuspto-grants-1998_05
ORD IDord-b36e3a7a120d43e28d98b3e077d35ae2
Source noteuspto-grants-1998_05