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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745898Generated: October 31, 2026

Sodium borohydride → HCID 57739004, compound

https://huagongshe.com/reaction/1745898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22227324HCID 22227324—
SolventNpc112006HCID 21965192—
ProductHCID 57739004HCID 5773900470%

Reaction Steps

To a solution of 4-(trifluorovinyloxy)benzaldehyde (about 35 mmol) in benzene/ethanol (75/75 mL) at room temperature was added sodium borohydride (1.8 g, 1.3 eq). The resulting mixture was stirred at room temperature for 3 h. Under reduced pressure, all the solvent was evaporated. The residue was extracted by CH2Cl2 for 1 h and dried over sodium sulfate. The product was purified by chromatography using CH2Cl2 as the eluent to afford 4-(trifluorovinyloxy)benzyl alcohol as colorless oil (5.0 g, yield 68%). 1H NMR (CDCl3): δ 7.36 (d, J=8.8 Hz, 2H), 7.09 (d, J=8.8 Hz, 2H), 4.67 (s, 2H), 2.03 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019453B2
Source datasetuspto-grants-2006_03
ORD IDord-11da16b25528478d88b02af9d5a4bac5
Source noteuspto-grants-2006_03