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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172856Generated: November 2, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 57443974, compound

https://huagongshe.com/reaction/1172856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 57443968HCID 57443968—
SolventMethanolHCID 887—
ProductHCID 57443974HCID 57443974—

Reaction Steps

A solution of 6-hydroxymethyl-benzo[b]thiophene-2-carboxylic acid ethyl ester (9.45 g, 40.0 mmol) and DBU (6.00 mL, 40.1 mmol) in anhydrous MeOH (200 mL) was allowed to stir for 2 d. After concentration, the residue was dissolved in EtOAc (800 mL) and washed with 1N HCl, water, saturated NaHCO3 and brine. The organic layer was dried, filtered and the filtrate was concentrated and dried to give 6-hydroxymethyl-benzo[b]thiophene-2-carboxylic acid methyl ester as off white solid. 1H NMR (CDCl3, 200 MHz) δ 8.03 (d, J=0.6 Hz, 1H), 7.90-7.80 (m, 2H), 7.39 (dd, J=8.0, 1.4 Hz, 1H), 4.83 (s, 2H), 3.94 (s, 3H), 1.98 (brs, 1H). MS (EI): cal'd 223.0 (MH+), exp 223.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834034B2
Source datasetuspto-grants-2010_11
ORD IDord-96d299d80711495485aaf45849b741d7
Source noteuspto-grants-2010_11