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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732588Generated: November 2, 2026

Acetaldehyde → 81244-91-9

https://huagongshe.com/reaction/1732588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantHCID 22813385HCID 22813385—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product81244-91-9HCID 1425483058.5%

Reaction Steps

A suspension of trans-4,6,6a,8,9,10a-hexahydro-7H-indolo-[3,4 gh]-[1,4]-benzoxazine (650 mg, 0.03 m) acetaldehyde (260 mg, 0.006 m) and Pd/c (10%, 700 mg) in abs. ethanol (50 ml) is hydrogenated at room temperature for 4 hours. The catalyst is removed by filtration, and the solvent is removed under reduced pressure (20 mm). The oil is recrystallized from methanol to yield 430 mg of trans 4,6,6a,8,9,10a-hexahydro-7-ethyl-7H-indolo-[3,4 gh]-[1,4]benzoxazine, m.p. turns brown 200° melt 210°-213°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238486
Source datasetuspto-grants-1980_12
ORD IDord-06e7e7f5280f4cf08c69511a09a0f74a
Source noteuspto-grants-1980_12