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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661834Generated: November 2, 2026

Sodium borohydride → HCID 66606820, compound

https://huagongshe.com/reaction/661834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68746412HCID 68746412—
SolventMethanolHCID 887—
ProductHCID 66606820HCID 6660682095%

Reaction Steps

Step 2 A suspension of 2-(3-bromo-2-methylphenyl)isoquinoline-1,3(2H,4H)-dione (630 mg, 1.908 mmol) in methanol (100 mL) was treated with sodium borohydride (217 mg, 5.72 mmol) at rt. After 1.5 h, additional sodium borohydride (120 mg) was added. After 7 h, the mixture was concentrated and the residue was partitioned between water and DCM. The organic phase was dried and concentrated to give 2-(3-bromo-2-methylphenyl)-3-hydroxy-3,4-dihydroisoquinolin-1(2H)-one as a light yellow foam (600 mg, 95%), used without further purification. Mass spectrum m/z 332, 334 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-e67c627a8b3c42afaf82a0f58ba486ca
Source noteuspto-grants-2011_12