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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821095Generated: October 31, 2026

Water → 2-(Benzyloxy)-5,6,7,8-tetrahydroquinolin-5-amine

https://huagongshe.com/reaction/1821095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoraneHCID 6331—
ReactantHCID 19026180HCID 19026180—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzyloxy)-5,6,7,8-tetrahydroquinolin-5-amineHCID 992131889%

Reaction Steps

A solution of O-benzyl-N-(2-benzyloxy-5,6,7,8-tetrahydro-quinolin-5-yl)-hydroxylamine (51.0 g, 142 mmoL) dissolved in dry THF (65 mL) was cooled in ice-water bath under nitrogen. Borane (1.0 M in THF, 427 mL) was added dropwise in 30 min via an addition funnel. The reaction was allowed to warm up to room temperature and stirred for overnight. The mixture was then heated to reflux. After 2 h, the heating was stopped and the reaction was allowed to cool to room temperature. Water (120 mL) was added dropwise via an addition funnel. The mixture was then concentrated, and 20% aqueous sodium hydroxide (200 mL) was added. The resulting mixture was heated to reflux for 2 h. The reaction was allowed to cool to room temperature, and extracted with methylene chloride (×3). The combined methylene chloride extract was dried, filtered and concentrated. Purification by column chromatography on silica gel with 20% methanol/1% ammonium hydroxide/methylene chloride provided the desired product (32.0 g, 89%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07605265B2
Source datasetuspto-grants-2009_10
ORD IDord-3c6206aae1034fabb2818b092cd23a96
Source noteuspto-grants-2009_10