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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252739Generated: October 30, 2026

Sodium cyanoborohydride → HCID 23400512, compound

https://huagongshe.com/reaction/2252739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69207073HCID 69207073—
SolventAcetic AcidHCID 176—
ProductHCID 23400512HCID 2340051249%

Reaction Steps

To a stirred solution of (S)-1-[2-(tert-butoxycarbonylamino)propyl]-benz[g]indole (0.49 g, 1.5 mmol) in acetic acid (10 mL) was added portionwise sodium cyanoborohydride (95%, 0.30 g, 4.5 mmol). The mixture was stirred for 16 h and partitioned between ether (40 mL) and saturated aqueous sodium bicarbonate solution (3×50 mL). The organic layer was washed with brine (2×), dried (magnesium sulfate), concentrated in vacuo and purified by column chromatography [SiO2; heptane-ethyl acetate (6:1)] to give the product (0.24 g, 49%) as a pale yellow solid: IR νmax (Nujol)/cm−1 1689, 1528, 1362, 1298, 1051 and 790; NMR δH (400 MHz, CDCl3) 1.39 (3H, d, J 6.5 Hz), 1.45 (9H, s), 3.11-3.28 (2H, m), 3.32-3.42 (2H, m), 3.62-3.69 (2H, m), 3.98-4.08 (1H, m), 4.78 (1H, brs), 7.30-7.38 (1H, m), 7.33-7.41 (3H, m), 7.72-7.81 (1H, m) and 7.98-8.01 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323473B2
Source datasetuspto-grants-2008_01
ORD IDord-fdd1075ff28f493b9f946c7d1d17a741
Source noteuspto-grants-2008_01