Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926220Generated: November 1, 2026

1,1-Difluoro-2-methylpropan-2-ol → 2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethanol

https://huagongshe.com/reaction/926220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-Difluoro-2-methylpropan-2-olHCID 23531634—
Reactant2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1,1-trifluoro-2-methylpropan-2-yloxy)ethanolHCID 89676680—
Product2-(1-Chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethanolHCID 89676545—

Reaction Steps

Compound 2-(1-chloro-3-methylnaphthalen-2-yl)-2-(1,1-difluoro-2-methylpropan-2-yloxy)ethanol was prepared following the procedure used to prepare 2-(1-chloro-3-methylnaphthalen-2-yl)-2-(1,1,1-trifluoro-2-methylpropan-2-yloxy)ethanol of Example 31, except that 1,1-difluoro-2-methylpropan-2-ol (10 eq) was used instead of 2-trifluoromethyl-2-propanol (25 eq). 1H-NMR: 400 MHz, (CDCl3) δ 8.27 (d, J=8.4 Hz, 1H), 7.73 (d, J=7.6 Hz, 1H), 7.57-7.49 (m, 3H), 5.85 (dd, J=9.2, 3.6 Hz, 1H), 5.61 (t, J=56.4 Hz, 1H), 3.94 (dd, J=11.6, 9.6 Hz, 1H), 3.65 (dd, J=11.6, 4.4 Hz, 1H), 2.69 (s, 3H), 2.18 (br s, 1H), 1.32 (s, 3H), 1.10 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284323B2
Source datasetuspto-grants-2016_03
ORD IDord-2053040a1ac44f6fb43a32ce1c1678a1
Source noteuspto-grants-2016_03