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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65299Generated: October 25, 2026

Sodium borohydride → 1-Nitrohexane

https://huagongshe.com/reaction/65299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantBoronHCID 5462311—
ReactantO-acetyl-1-(3,4-dimethoxyphenyl)-2-nitro-6-cyano-6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexan-3-olHCID 13745755—
ReactantNitrohexanol acetateHCID 88666005—
Product1-NitrohexaneHCID 12589—
Product1-(3,4-Dimethoxyphenyl)-2-nitro-6-cyano-6-(prop-2-yl)-6-(3,4-dimethoxyphenyl)hexaneHCID 13745756—

Reaction Steps

The resulting nitrohexanol acetate of formula 9 is then reduced using a boron-based reducing agent, e.g., sodium borohydride, in a 2° or 3° alkanol at 25°-80° C. for 3-15 hours to produce a nitrohexane derivative of formula 10 (step 8). For example, O-acetyl-1-(3,4-dimethoxyphenyl)-2-nitro-6-cyano-6-(i-propyl)-6-(3,4-dimethoxyphenyl)hexan-3-ol (9) is heated with NaBH4 in 2-propanol at reflux for 3-15 hours to yield 1-(3,4-dimethoxyphenyl)-2-nitro-6-cyano-6-(prop-2-yl)-6-(3,4-dimethoxyphenyl)hexane (10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613606
Source datasetuspto-grants-1986_09
ORD IDord-5996a0cb552e4bc3b85ddb845d7c6fa3
Source noteuspto-grants-1986_09