Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696295Generated: November 2, 2026

Acetic Acid → HCID 77174872, compound

https://huagongshe.com/reaction/1696295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopentanoneHCID 8452—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant3,4-dihydro-2H-1,4-benzoxazine-2-carboxylic acidHCID 3826952—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 77174872HCID 77174872—

Reaction Conditions

Temperature25 °C

Reaction Steps

Cyclopentanone (83 L, 0.94 mmol), acetic acid (54 L, 0.94 mmol), and magnesium sulfate (113 mg, 0.94 mmol) were added to a solution of (±)-3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylic acid (Example 3a, 65 mg, 0.31 mmol) in dichloroethane (1.25 mL). Sodium triacetoxyborohydride (100 mg, 0.47 mmol) was added, followed by dichloroethane (1.25 mL), and the suspension was stirred at 25° C. for 48 h. The reaction mixture was quenched with half-saturated sodium bicarbonate, and the product was extracted using 67% EtOAc/hexane (3×25 mL). The combined organic fractions were dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (10% EtOAc/hexane) afforded the title compound as an oil. MS m/z: 276 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163766B2
Source datasetuspto-grants-2012_04
ORD IDord-3326df04580f4a8882341067f04b2478
Source noteuspto-grants-2012_04