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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178387Generated: October 31, 2026

Sodium borohydride → HCID 118114009, compound

https://huagongshe.com/reaction/2178387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12439091HCID 12439091—
SolventMethanolHCID 887—
ProductHCID 118114009HCID 11811400985%

Reaction Steps

To a stirred 0° C. solution of 3-methoxy-6,7-dihydroisoquinolin-8(5H)-one (1.90 g, 10.72 mmol) in methanol (30 mL) was added sodium borohydride (1.10 g, 29.08 mmol) in small portions. The resulting mixture was allowed to warm to room temperature. After 2 h, the mixture was quenched with water (20 mL) and was extracted with ethyl acetate (3×100 mL). The combined organic phases were dried over sodium sulfate, filtered, and concentrated. Chromatographic purification of the residue (silica gel, 50% ethyl acetate in petroleum ether elute) afforded 1.60 g (85%) of 3-methoxy-5,6,7,8-tetrahydroisoquinolin-8-ol as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067914B1
Source datasetuspto-grants-2015_06
ORD IDord-b2165403630f44d8b3c100203b0cccf9
Source noteuspto-grants-2015_06