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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496914Generated: October 31, 2026

Sodium borohydride → 2-(4-(Trifluoromethoxy)phenyl)pyrimidine-5-methanol

https://huagongshe.com/reaction/1496914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-(4-(Trifluoromethoxy)phenyl)pyrimidine-5-carboxaldehydeHCID 49852139—
SolventMethanolHCID 887—
Product2-(4-(Trifluoromethoxy)phenyl)pyrimidine-5-methanolHCID 2320783784.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

NaBH4 (0.22 g, 5.82 mmol) was added to a solution of aldehyde 90 (0.776 g, 2.89 mmol) in MeOH (100 mL) at 0° C. The solution was stirred at 0° C. for 1 h, then quenched with brine and partitioned between EtOAc and water. Column chromatography of the organic portion on silica gel (eluting with 1:1 EtOAc/hexanes) gave {2-[4-(trifluoromethoxy)phenyl]-5-pyrimidinyl}methanol (91) (0.657 g, 84%) as a white solid: mp 84-85° C.; 1H NMR [(CD3)2SO] δ 8.86 (s, 2H), 8.50 (d, J=8.9 Hz, 2H), 7.51 (d, J=8.9 Hz, 2H), 5.46 (t, J=5.5 Hz, 1H), 4.60 (d, J=5.5 Hz, 2H). APCI MS m/z 271 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09198913B2
Source datasetuspto-grants-2015_12
ORD IDord-cebb486e7858427592fc66ec745ee48c
Source noteuspto-grants-2015_12