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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726865Generated: November 1, 2026

Sodium borohydride → HCID 57565070, compound

https://huagongshe.com/reaction/1726865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57565084HCID 57565084—
SolventMethanolHCID 887—
ProductHCID 57565070HCID 57565070—

Reaction Steps

To a solution of (Z)-1-phenylcyclohept-4-enecarbaldehyde (22 mg, step C) in methanol (1 mL) was added sodium borohydride (8 mg), and the resulting mixture was stirred at room temperature for 1 h. Methanol was removed in vacuo, water and ethyl acetate were added. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate and filtered. The filtrate was evaporated in vacuo to give the title compound as an oil. 1H NMR (400 MHz, CDCl3) δ 1.91 (2H, m), 2.20 (6H, m), 3.55 (2H, s), 5.68 (2H, m), 7.35 (5H, m). 13C NMR (CDCl3, 100 MHz) δ 24.0, 32.9, 47.3, 71.7, 126.3, 127.4, 128.6, 131.2, 144.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494986B2
Source datasetuspto-grants-2009_02
ORD IDord-ec1b5e22fe014bc7b69d84c5dd315300
Source noteuspto-grants-2009_02