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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926221Generated: November 1, 2026

2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1,1-trifluoro-2-methylpropan-2-yloxy)ethyl pivalate → 2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethyl pivalate

https://huagongshe.com/reaction/926221

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1,1-trifluoro-2-methylpropan-2-yloxy)ethyl pivalateHCID 89676509—
Reactant2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethanolHCID 89676545—
Product2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethyl pivalateHCID 89676475—

Reaction Steps

Compound 2-(1-chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethyl pivalate was prepared following the procedure used to prepare 2-(1-chloro-3-methylnaphthalen-2-yl)-2-(1,1,1-trifluoro-2-methylpropan-2-yloxy)ethyl pivalate of Example 31, except that 2-(1-chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethanol was used instead of 2-(1-chloro-3-methylnaphthalen-2-yl)-2-(1,1,1-trifluoro-2-methylpropan-2-yloxy)ethanol. 1H-NMR: 400 MHz, (CDCl3) δ 8.27 (d, J=8.0 Hz, 1H), 7.73 (d, J=8.8 Hz, 1H), 7.57 (s, 1H), 7.56-7.50 (m, 2H), 6.01 (dd, J=8.4, 4.8 Hz, 1H), 5.53 (t, J=56.4 Hz, 1H), 4.47 (dd, J=11.6, 8.4 Hz, 1H), 4.19 (dd, J=11.6, 5.6 Hz, 1H), 2.72 (s, 3H), 1.27 (s, 6H), 1.16 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284323B2
Source datasetuspto-grants-2016_03
ORD IDord-cfcfa75cafad48cea26459f67a7abad4
Source noteuspto-grants-2016_03