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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222623Generated: November 1, 2026

Sodium borohydride → HCID 86593507, compound

https://huagongshe.com/reaction/2222623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86637625HCID 86637625—
SolventMethanolHCID 887—
ProductHCID 86593507HCID 8659350794%

Reaction Steps

To a solution of 6a (420 mg, 1.4 mmol) in methanol (10 mL) was added NaBH4 (531 mg, 14.0 mmol) in small portions. The reaction mixture was stirred at room temperature for 1 h before removal of the solvent. The residue was partitioned between 100 mL of ethyl acetate and 50 mL of water. The aqueous layer was extracted with 100 mL of ethyl acetate. The combined organic layers were dried over Na2SO4 and concentrated to yield 357 mg of the desired product as a white solid (94%). 1H NMR (300 MHz, CDCl3) δ 4.74 (m, 1H), 3.71 (m, 2H), 3.58 (m, 1H), 2.31 (m, 1H), 2.14 (m, 1H), 1.92 (m, 1H), 145 (s, 9H), 1.17 (d, 3H, J=7.0 Hz). 13C NMR (75.5 MHz, CDCl3) δ 156.26 (C═O), 128.41 (q, CF3, 1JCF=279.4 Hz), 80.14 (C), 64.78 (CH2), 50.73 (CH), 35.59 (q, CH, 2JCF=29.6 Hz), 31.74 (CH2), 28.52 (3×CH3), 13.71 (CH3); 19F NMR (282.6 MHz, CDCl3/CFCl3) δ −73.84 (br. s, 3F); GC-MS (CI, CH4): 272 (100, [M+1]+), 216 (68), 172 (26), 57 (11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371867B2
Source datasetuspto-grants-2008_05
ORD IDord-69d7e914e6c447099a7d7210ad1cb5ff
Source noteuspto-grants-2008_05