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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348913Generated: October 30, 2026

Citric Acid → HCID 17965983, compound

https://huagongshe.com/reaction/1348913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 90994751HCID 90994751—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17965983HCID 17965983—

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of Example 93B (2.15 g, 78% potency, 4.24 mmol) in THF (6.5 mL) was treated with a solution of 2M LiBH4 in THF (3.3 mL, 6.1 mmol), heated to 55° C. for 3 hours, cooled to room temperature, treated with 20% citric acid (12 mL), warmed to 50° C. for 30 minutes, and extracted with MTBE (2×20 mL). The aqueous phase was adjusted to pH>10 with 50% NaOH and extracted with 5:1 THF/ethyl acetate (2×30 mL). The combined organic phases were concentrated, treated with citric acid (1.0 g), and concentrated to a volume of approximately 6 mL. The solution was adjusted to pH>10 with 50% NaOH, stirred for 2 hours, and filtered. The filter cake was washed with water (2 mL) and dried under vacuum with an air bleed to provide 670 mg (61% potency, 40% potency adjusted yield) of the desired product as one enantiomer in high excess. MS (ACPI) m/e 244 (M+H)+; 1H NMR (CD3OD) δ 7.70 (d, 2H) 7.55 (s, 1H) 7.54 (d, 2H) 7.18 (s, 1H) 4.00 (d, 1H) 3.89 (d, 1H) 3.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211595B2
Source datasetuspto-grants-2007_05
ORD IDord-ddcfeeca599f4fb1a6210c7e32e2ab4e
Source noteuspto-grants-2007_05