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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370448Generated: October 31, 2026

Ethyl Acetate → HCID 22396830, compound

https://huagongshe.com/reaction/1370448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 22396583HCID 22396583—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22396830HCID 2239683087.3%

Reaction Steps

A solution of tert-butyl 7,9-dichloro-6-(2-ethoxy-2-oxoethyl)-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate (3.00 g, 6.80 mmol) in dry THF (30 mL) was cooled to 0° C. Then, LiBH4 (0.44 g, 20.2 mmol) was added and the reaction was allowed to warm slowly to rt. After 18 h, additional LiBH4 (0.44 g, 20.2 mmol) was added. After an additional 24 h, the reaction was diluted with H2O followed by addition of 10% aqueous NaOH and extraction with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, decanted, and concentrated. The crude product was first purified by column chromatography (Biotage 40M, SIM) with heptane/EtOAc (1:1) to give 2.37 g of impure product. Then, crystallization from EtOAc/heptane gave 2.21 g (82%) of ivory crystals: mp 183-184° C.; IR (diffuse reflectance) 1693, 1658, 1468, 1448, 1433, 1406, 1380, 1370, 1347, 1323, 1293, 1226, 1166, 1064, 771 cm1; MS (EI) m/z 398 (M+), 344, 342, 270, 268, 258, 256, 63, 57, 56. Anal. Calcd for C19H24Cl2N2O3: C, 57.15; H, 6.06; N, 7.01; found: C, 57.20; H, 6.11; N, 6.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583135B2
Source datasetuspto-grants-2003_06
ORD IDord-662c852083264f5e98fe197c5d92d55f
Source noteuspto-grants-2003_06