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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381212Generated: November 4, 2026

Sodium borohydride → HCID 49806571, compound

https://huagongshe.com/reaction/2381212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 49806452HCID 49806452—
SolventMethanolHCID 887—
ProductHCID 49806571HCID 4980657183%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 9,10-dimethoxy-8,8-dimethyl-5,8-dihydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline (600 mg, 1.64 mmol) in methanol (50 mL) was added sodium borohydride (65 mg, 1.7 mmol) in small portions at 0° C. After stirring at 0° C. for 2 h, the mixture was concentrated in vacuo. The resulting residue was extracted with diethyl ether (2×50 mL), washed with water (2×25 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to afford 9,10-dimethoxy-8,8-dimethyl-5,8,13,13a-tetrahydro-6H-[1,3]dioxolo[4,5-g]isoquino[3,2-a]isoquinoline (0.5 g, 83%). LC/MS m/e calcd for C22H25NO4 (M+H)+: 368.45, observed: 368.1; 1H NMR (400 MHz, MeOD) δ ppm 1.51 (s, 3 H) 1.72 (s, 3 H) 2.63-2.84 (m, 3 H) 2.84-2.93 (m, 1 H) 3.06 (dd, J=16.17, 3.79 Hz, 1 H) 3.21-3.28 (m, 1 H) 3.83 (s, 3 H) 3.86 (s, 3 H) 4.09 (dd, J=11.37, 3.54 Hz, 1 H) 5.88 (s, 2 H) 6.58 (s, 1 H) 6.75 (s, 1 H) 6.80-6.85 (m, 1 H) 6.86-6.91 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258149B2
Source datasetuspto-grants-2012_09
ORD IDord-fee61bcd512a482b80884a2e9e6b5126
Source noteuspto-grants-2012_09