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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75723Generated: October 29, 2026

Methanol → HCID 67225989, compound

https://huagongshe.com/reaction/75723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl 8-fluoro-1,4-dioxaspiro[4.5]decane-8-carboxylateHCID 67960160—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67225989HCID 6722598956%

Reaction Steps

To a solution of crude ethyl 8-fluoro-1,4-dioxaspiro[4.5]decane-8-carboxylate, Intermediate 30, (16.26 g, 70 mmol calculated based on previous reaction, 1 equiv) in THF (100 mL) was added LiBH4 (45.5 mL of a 2 M solution in THF, 91 mmol, 1.3 equiv) followed by MeOH (3.68 mL, 91 mmol, 1.3 equiv). Significant warming was observed following MeOH addition. The reaction was stirred 30 min at which time TLC showed no ester remaining. The reaction was poured into a saturated aqueous solution of NaHCO3 and the aqueous solution was extracted with ether (×3). The combined ether layers were dried (MgSO4) and concentrated in vacuo. The crude product was purified by silica gel chromatography (30-90% ethyl acetate/hexane) to provide the title compound (7.50 g, 56% yield for 2 steps) as a pale yellow oil. 1H NMR (400 MHz, CDCl3) δ ppm 3.90-4.03 (m, 4H), 3.64 (d, J=6.78 Hz, 1H), 3.59 (d, J=6.78 Hz, 1H), 1.97-2.09 (m, 2H), 1.84-1.95 (m, 2H), 1.62-1.80 (m, 4H); 19F NMR (376 MHz, CDCl3) δ ppm −171.25 (br. s., 1F).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835411B2
Source datasetuspto-grants-2014_09
ORD IDord-5a876810e4d94988af54b4bb03411aa1
Source noteuspto-grants-2014_09