Benzyl vinylcarbamate Chemical Properties

Melting point:

43-44°C

Boiling point:

272℃

Density 

1.089

Flash point:

118℃

storage temp. 

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

solubility 

Chloroform (Slightly), Ethyl Acetate (Slightly)

form 

Solid

pka

11.04±0.46(Predicted)

color 

White to Off-White

Safety Information

Risk Statements 

36/37/38

Safety Statements 

26-36/37/39

Benzyl vinylcarbamate Usage And Synthesis

Uses

Benzyl Vinylcarbamate is used as a reagent in the synthesis of CF3- or -?CF2-?substituted tetrahydroquinolines.

Preparation

A 1-L flask was equipped with a variable speed pump, a mechanical stirrer, a temperature controller, a 4" (10 cm) column packed with ceramic saddles, a distillation head, a spiral condenser (cooled with water at 10–15 ℃), and a receiver. The flask was charged with toluene (150–200 mL) and phenothiazine (0.5 g) and the solution was heated to 105–110 ℃. The receiver was charged with benzyl alcohol (86 g, 0.8 mol), phenothiazine (0.05 g), and triethylamine (0.1–0.3 g). This mixture was cooled in ice and stirred. A solution of acryloyl azide (1 mol), prepared as described above, was pumped into the distillation flask over a period of 4–5 h, maintaining the pot temperature at 105–110 ℃ with a heating mantle. The vapor temperature varied, depending on the rate of addition of the azide, but was in the range 80–100 ℃. The distillate was passed directly into the benzyl alcohol mixture. After the addition of acryloyl azide, the distillation continued, generating a further 10–20 mL of toluene. The receiver was then removed from the distillation set-up, and its contents were stirred at 0–5 ℃ for 1– 2 h. The product mixture was then allowed to gradually warm to room temperature and was stirred until HPLC analysis indicated complete reaction. The mixture was then concentrated in vacuo to a weight of 200–250 g. The residue was treated with heptane (300–350 mL) and cooled to 15 ℃ with stirring. A few seed crystals of benzyl N-vinyl carbamate 810 were added, and the mixture was stirred for 2–3 h. The product was collected by filtration, washed with heptane, and dried in vacuo. Yield 115–128 g (65–72%); mp 41–44 ℃.

Application

Benzyl-N-vinyl carbamate (Z-vinylamine; Benzyl vinylcarbamate) is a valuable synthetic intermediate. This compound undergoes alkylation readily on the carbon R to the nitrogen, a property that has been used in the synthesis of a-lactam antibiotics. Z-vinylamine can be readily polymerized into polyvinyl amine derivatives[1].

Synthesis Reference(s)

The Journal of Organic Chemistry, 54, p. 4649, 1989 DOI: 10.1021/jo00280a036

References

[1] Govindan, Cheruthur K. “An Improved Process for the Preparation of Benzyl-N-vinyl Carbamate1.” Organic Process Research Development 6 1 (2001): 74–77.

Benzyl vinylcarbamate(84713-20-2)Related Product Information

• Z-DEHYDRO-ALA-OME
• Z-DEHYDRO-ALA-OH
• BENZYL N-STYRYLCARBAMATE
• 2,3,4,5,6-PENTAMETHYLBENZYL N-(1,2,2-TRICHLOROVINYL)CARBAMATE
• 3-CHLOROBENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 4-(TRIFLUOROMETHYL)BENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 4-ISOPROPYLBENZYL N-(1,2,2-TRICHLOROVINYL)CARBAMATE
• 4-CHLOROBENZYL N-STYRYLCARBAMATE
• 2,6-DICHLOROBENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 2,6-DICHLOROBENZYL N-STYRYLCARBAMATE
• 2,4-DICHLOROBENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 4-(TERT-BUTYL)BENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 4-BROMOBENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 4-METHOXYBENZYL N-STYRYLCARBAMATE
• 4-METHOXYBENZYL N-[2-(2-FURYL)VINYL]CARBAMATE
• 4-CHLORO-3-NITROBENZYL N-(1,2,2-TRICHLOROVINYL)CARBAMATE
• 4-METHOXYBENZYL N-(4-CHLOROSTYRYL)CARBAMATE
• 4-CHLOROBENZYL N-[2-(2-FURYL)VINYL]CARBAMATE