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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925231Generated: October 28, 2026

Sulfuric Acid → 7-Hydroxy-1,2,4,5-tetrahydro-benzo[d]azepine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/925231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium NitriteHCID 23668193—
Reactant7-Amino-1,2,4,5-tetrahydro-benzo[d]azepine-3-carboxylic acid ethyl esterHCID 58494878—
SolventWaterHCID 962—
Product7-Hydroxy-1,2,4,5-tetrahydro-benzo[d]azepine-3-carboxylic acid ethyl esterHCID 5849536366.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

Into a 250 ml flask, the product from step (b) (3 g, 12.82 mmol) dissolved in water (15 ml) and concentrated H2SO4 (1.02 ml, 19.23 mmol) was added The reaction mixture was heated to 70° C. and stirred for 15 minutes. A solution of NaNO2 (1.01 g, 14.74 mmol) in water (30 ml) was quickly added, followed by addition of THF (45 ml). The reaction mixture was stirred at 70° C. for 30 minutes and then allowed to cool to room temperature. The reaction mixture was extracted with EtOAc (3×). The combined EtOAc extracts were washed with brine, dried over Na2SO4, and solvent evaporated in vacuo to give the sub-title compound as a yellow solid (2.0 g) that was used without further purification. MS: ESI (positive): 236 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284277B2
Source datasetuspto-grants-2016_03
ORD IDord-c25dd445368a43d193e3442023421bb5
Source noteuspto-grants-2016_03