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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990399Generated: October 31, 2026

Sodium triacetoxyborohydride → (S)-(1-{[4,4-Bis-(4-fluoro-phenyl)-butylamino]-methyl}-3-methyl-butyl)-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/990399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 13530069HCID 13530069—
Reactant(S)-(1-Formyl-3-methyl-butyl)-methyl-carbamic acid tert-butyl esterHCID 54220075—
SolventEthyl AcetateHCID 8857—
Product(S)-(1-{[4,4-Bis-(4-fluoro-phenyl)-butylamino]-methyl}-3-methyl-butyl)-methyl-carbamic acid tert-butyl esterHCID 5412540970.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

4,4-bis-(4-fluorophenyl)-butylamine (200 mg, 0.77 mmol) was dissolved in CH,2Cl2 (5 mL), treated with (S)-(1-formyl-3-methyl-butyl)-methyl-carbamic acid tert-butyl ester (229 mg, 1.0 mmol), stirred for 30 minutes, then cooled to 0° C., treated with NaBH(OAc)3 (245 mg, 1.16 mmol), and stirred overnight at room temperature. The reaction was diluted with EtOAc (100 mL), washed with saturated bicarbonate solution and brine, dried over Na2SO4, and concentrated. The crude material was chromatographed on silica gel eluting with 4% MeOH/CH2Cl2 to give 257 mg (70%) of the desired product as an oil. MS: 475.4 (M+1 for C28H40N2O2F2); an oil; TLC (SiO2), Rf 0.26 (4% MeOH/CH2Cl2); HPLC (1:1 CH3CN/H2O with 0.1% TFA, C-18 column) 100%, RT=15.013 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458781B1
Source datasetuspto-grants-2002_10
ORD IDord-5d77ad6fed0f43758ee948cbb70c46b3
Source noteuspto-grants-2002_10