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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556169Generated: October 30, 2026

tert-butyl-1-((S)-4-(3,4-dichlorophenyl)-3,4-dihydronaphthalen-2-yl)ethylcarbamate → tert-butyl 1-((2S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-2-yl)ethylcarbamate

https://huagongshe.com/reaction/556169

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl-1-((S)-4-(3,4-dichlorophenyl)-3,4-dihydronaphthalen-2-yl)ethylcarbamateHCID 66808903—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Producttert-butyl 1-((2S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-2-yl)ethylcarbamateHCID 5895074868%

Reaction Steps

To a solution of tert-butyl (S)-1-((S)-4-(3,4-dichlorophenyl)-3,4-dihydronaphthalen-2-yl)ethylcarbamate 49a (Example 21.3) (60 mg, 0.14 mmol) in ethyl acetate (8 mL) was added palladium on charcoal (30 mg, 5%). The mixture was then stirred under hydrogen (1 atm) for 1 h. The catalyst was filtered off through a pad of Celite. The filtrate was concentrated. Chiral AD column separation (ethanol/methanol/hexane/DEA=3:2:95:0.1) afforded tert-butyl 1-((2S,4S)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-2-yl)ethylcarbamate (isomer 2) (40 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053603B2
Source datasetuspto-grants-2011_11
ORD IDord-0908f9d286d046639144cecffd6421fe
Source noteuspto-grants-2011_11