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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531285Generated: October 31, 2026

Nitric Acid → HCID 20772336, compound

https://huagongshe.com/reaction/1531285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 86588387HCID 86588387—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 20772336HCID 20772336—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 90% HNO3 (55.1 g, 0.8 mol) under nitrogen at −30° C. is added 100 mL of trifluoroacetic acid followed by the addition of trifluoroacetic anhydride (100 g, 0.476 mol) over 5 minutes. The above carbamate (1-acetyloxy-indan-2-yl)-carbamic acid methyl ester (1S-trans)) (20.0 g, 0.08 mol) in 34 mL of methylene chloride is added slowly (over 90 min.) keeping the temperature between −30 and −35° C. The reaction is worked up by adding 100 mL of water and warmed to 0° C. to give two layers. The layers are separated and the aqueous layer extracted with methylene chloride. The combined organic extracts are washed with 100 mL of water (pH is adjusted to 8.5 with sodium bicarbonate), and with cold water. The organic layer is dried over MgSO4, filtered and evaporated to give crude product. The crude product is crystallized from ethyl acetate and further precipitated by the addition of heptane to give (1-acetyloxy-6-nitro-indan-2-yl)-carbamic acid methyl ester (1S-trans); mp 164-167° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197798B1
Source datasetuspto-grants-2001_03
ORD IDord-210aac2cfa174e67bea3f1881d7c28aa
Source noteuspto-grants-2001_03