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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628627Generated: October 30, 2026

HCID 68938318, compound → HCID 68943450, compound

https://huagongshe.com/reaction/628627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68938318HCID 68938318—
ReactantHCID 178418287HCID 178418287—
ProductHCID 68943450HCID 68943450—

Reaction Steps

(E)-Tert-butyl 3-hydroxy-2,2-dimethyl-3-(3-(2-(2,6,6-trimethylcyclohex-1-enyl)vinyl)phenyl)propylcarbamate (0.0809 g, 0.19 mmol) was reacted with pyridinium chlorochromate according to the method used in Example 56 except that the reaction time was 2 h, 15 min. Purification by flash chromatography (10 to 40% EtOAc-hexanes gradient) gave (E)-tert-butyl 2,2-dimethyl-3-oxo-3-(3-(2-(2,6,6-trimethylcyclohex-1-enyl)vinyl)phenyl)propylcarbamate as an oil. 1H NMR (400 MHz, CD3OD) δ 7.72 (s, 1H), 7.58 (d, J=7.6 Hz, 1H), 7.52 (d, J=8.0 Hz, 1H), 7.35 (t, J=7.6 Hz, 1H), 6.72 (dd, J=16.0, 0.8 Hz, 1H), 6.33 (d, J=16.0 Hz, 1H), 5.05 (t, J=6.0 Hz, 1H), 3.38 (d, J=6.8 Hz, 2H), 2.04 (t, J=6.4 Hz, 2H), 1.76 (s, 3H), 1.61-1.67 (m, 2H), 1.48-1.50 (m, 2H), 1.36-1.42 (m, 15H), 1.06 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09314467B2
Source datasetuspto-grants-2016_04
ORD IDord-97835eded7ff48398a2a583dccf8e390
Source noteuspto-grants-2016_04