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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220348Generated: October 26, 2026

Sodium borohydride → 1-(Benzyl-methyl-amino)-heptan-3-ol

https://huagongshe.com/reaction/2220348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(Benzyl-methyl-amino)-heptan-3-oneHCID 17981922—
SolventMethanolHCID 887—
Product1-(Benzyl-methyl-amino)-heptan-3-olHCID 1798193394.3%

Reaction Steps

Add sodium borohydride (1.29 g, 34.1 mmol) to a stirred solution of 1-(benzyl-methyl-amino)-heptan-3-one (2.41 g, 10 mmol) and methanol (45ml) at 0° C. under N2. Stir the reaction for 1 hr at 0° C. Quench the reaction with water at 0° C. and concentrate under reduced pressure. Dissolve the residue in ethyl acetate, wash with brine and dry over sodium sulfate. Filter off and concentrate to give the crude compound. Purify the compound by flash chromatography, eluting with 5% ethanol/0.5% ammonium hydroxide/chloroform to yield 2.22 g (91%) of 1-(benzyl-methyl-amino)-heptan-3-ol: mass spectrum (ion spray) m/z=236 (M+1); 1H NMR (CDCl3) δ 7.3-7.23 (m, 5H), 3.76-3.72 (m, 1H), 3.53 (dd, 2H), 2.80-2.73 (m, 1H), 2.59-2.53 (m, 1H), 2.21 (s, 3H), 1.68-1.62 (m, 1H), 1.57-1.29 (m, 7H), 0.91 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417064B2
Source datasetuspto-grants-2008_08
ORD IDord-ee43709c934f4ecf83312c785f65c3ac
Source noteuspto-grants-2008_08