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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716536Generated: November 2, 2026

Dichloromethane → (S)-{2-[6-(4-Methoxy-phenyl)-2,3-dihydro-indol-1-yl]-1-methyl-ethyl}-carbamic-Acid Tert-Butyl Ester

https://huagongshe.com/reaction/1716536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-{2-[6-(4-Methoxy-phenyl)-indol-1-yl]-1-methyl-ethyl}-carbamic acid tert-butyl esterHCID 67031552—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product(S)-{2-[6-(4-Methoxy-phenyl)-2,3-dihydro-indol-1-yl]-1-methyl-ethyl}-carbamic-Acid Tert-Butyl EsterHCID 2076196093.9%

Reaction Steps

(S)-{2-[6-(4-Methoxy-phenyl)-indol-1-yl]-1-methyl-ethyl}-carbamic acid tert-butyl ester (1.80 g) was dissolved in acetic acid (25 mL) and CH2Cl2 (10 mL) and cooled to 0° C. NaCNBH3 (1.41 g) was added in portions and the resulting mixture was allowed to stir for 4 hours. The reaction mixture was diluted with ethyl acetate and extracted with concentrated NaOH solution. The organic layer washed with brine, dried (Na2SO4) and evaporated. The residue was purified by flash chromatography (gradient of ethyl acetate in hexanes) to give the title compound as a brown oil (1.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803819B2
Source datasetuspto-grants-2010_09
ORD IDord-eff75cf5657d4db982bad1d17b9ff0d0
Source noteuspto-grants-2010_09