(Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

Base Information

Chemical Name:(Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate
CAS No.:196940-65-5
Molecular Formula:C₂₀H₂₉NO₃
Molecular Weight:331.455
Hs Code.:

Synonyms:(Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

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Chemical Property of (Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

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Technology Process of (Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

There total 3 articles about (Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

: 100-52-7
benzaldehyde

: [5-(2,2,4,4-tetramethyl-1,3-oxazolidine-3-carbonyloxy)pentyl]triphenylphosphonium bromide

: 196940-65-5
(Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

Guidance literature:: With potassium tert-butylate; In diethyl ether; at -40 ℃; for 0.0833333h;
DOI:10.1002/(SICI)1522-2675(19991110)82:11<1860::AID-HLCA1860>3.0.CO;2-8

Reference yield:

: 196940-78-0
5-bromopentyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

: 196940-65-5
(Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / 5 h / 100 °C

2: 86 percent / t-BuOK / diethyl ether / 0.08 h / -40 °C

With potassium tert-butylate; In diethyl ether; 1: Substitution / 2: Condensation;
DOI:10.1002/(SICI)1522-2675(19991110)82:11<1860::AID-HLCA1860>3.0.CO;2-8

Reference yield:

: 257629-47-3
5-hydroxypentyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

: 196940-65-5
(Z)-6-phenylhex-5-enyl 2,2,4,4-tetramethyl-1,3-oxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / CBr₄; PPh₃ / CH₂Cl₂ / 0.17 h / 0 °C

2: 95 percent / 5 h / 100 °C

3: 86 percent / t-BuOK / diethyl ether / 0.08 h / -40 °C

With carbon tetrabromide; potassium tert-butylate; triphenylphosphine; In diethyl ether; dichloromethane; 1: Substitution / 2: Substitution / 3: Condensation;
DOI:10.1002/(SICI)1522-2675(19991110)82:11<1860::AID-HLCA1860>3.0.CO;2-8