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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785885Generated: October 26, 2026

Acetaldehyde → HCID 58859730, compound

https://huagongshe.com/reaction/1785885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantAnilineHCID 6115—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium SulfateHCID 24436—
Reactantbenzyl N-ethenylcarbamateHCID 10931982—
SolventDichloromethaneHCID 6344—
ProductHCID 58859730HCID 5885973033.8%

Reaction Conditions

Temperature-25 °C

Reaction Steps

Aniline (3.64 mL, 39.97 mmol, 1.0 equ) was dissolved in methylene chloride (100 mL) and Na2SO4 (2 g) was added and cooled to −25° C. Acetaldehyde (2.23 mL, 39.97 mmol, 1.0 equ.) was added to the solution and stirred for 1 h at −25° C. Sodium sulfate was filtered off and N-vinyl-carbamic acid benzyl ester (7.07 g, 39.97 mmol, 1.0 equiv) was added to the filtrate at −25° C., followed by boron triflouride diethyl etherate (0.50 mL, 3.9 mmol, 0.1 equ). The reaction was allowed to stir at −25° C. for 1 h and then warmed to room temperature and stirred for 10 h. The reaction was evaporated in vacuo and the residue was purified by Biotage flash system (20% ethyl acetate/80% hexane) to yield 4.0 g, 33% of (±)-cis-(2-methyl-1,2,3,4-tetrahydro-quinolin-4-yl)-carbamic acid benzyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504508B2
Source datasetuspto-grants-2009_03
ORD IDord-06f6d363cb3f4d8fbdd4a0ddadbf7f8f
Source noteuspto-grants-2009_03