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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904766Generated: November 2, 2026

Acetic Acid → HCID 20197302, compound

https://huagongshe.com/reaction/1904766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 14326577HCID 14326577—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20197302HCID 20197302104.3%

Reaction Steps

A solution of 3-[2-[[(phenylmethoxy)carbonyl]amino]ethyl]-1H-indole-5-carboxylic acid (9 g) and carbonyldiimidazole (5.2 g) in dry tetrahydrofuran (THF) (150 ml) was stirred vigorously under nitrogen at room temperature for 5 h. A solution of lithium borohydride (1.6 g) in dry THF (70 ml) was added over 70 min and the mixture then stirred for 18 h. Aqueous acetic acid (30%, 25 ml) was added slowly to the ice-cooled mixture and the solution was then partitioned between brine (25%, 300 ml) and ethyl acetate (250 ml). The organic layer was washed with sulphuric acid (0.4M, saturated with sodium chloride, 3×80 ml), brine (100 ml) and potassium carbonate solution (25%, 2×100 ml). The dried (MgSO4) solution was evaporated in vacuo, the residue taken up in dichloromethane (150 ml) and insoluble material was filtered off. The filtrate was evaporated in vacuo to leave the alcohol (9 g) as a colourless oil containing some (ca. 45 mole %) ethyl acetate. T.l.c. Si02 /Et2O, Rf 0.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04839377
Source datasetuspto-grants-1989_06
ORD IDord-c11e1ec54b8b4d6a90bea9e5129764c0
Source noteuspto-grants-1989_06