(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

Base Information

Chemical Name:(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane
CAS No.:127251-07-4
Molecular Formula:C₂₄H₃₂O₄Si
Molecular Weight:412.601
Hs Code.:

Synonyms:(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

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Chemical Property of (4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

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Technology Process of (4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

There total 6 articles about (4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane 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: 78.0%

: 169871-39-0
(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-(2-hydroxylethyl)-1,3-dioxolane

: 127251-07-4
(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -70 ℃; for 0.25h;
DOI:10.1016/0223-5234(96)88240-7

Reference yield:

: 73346-74-4
(4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-dimethanol

: 127251-07-4
(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) NaH / 1.) THF, 45 min, RT, 2.) THF, 45 min

2: 85 percent / oxalyl chloride, DMSO / CH₂Cl₂ / 0.25 h / -70 °C

3: 1.) nBuLi / 1.) THF, hexane, 30 min, 2.) THF, hexane, a) -25 deg C, 30 min, b) 1 h, RT

4: 1.) 9-BBN, 2.) aq. H₂O₂, NaOH / 1.) THF, RT, 1 h, 2.) EtOH, 15 min

5: 78 percent / oxalyl chloride, DMSO / CH₂Cl₂ / 0.25 h / -70 °C

With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; oxalyl dichloride; dihydrogen peroxide; sodium hydride; dimethyl sulfoxide; In dichloromethane;
DOI:10.1016/0223-5234(96)88240-7

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 127251-07-4
(4R,5R)-trans-2,2-dimethyl-4-tert-butyldiphenylsiloxymethyl-5-formylmethyl-1,3-dioxolane

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) NaH / 1.) THF, 45 min, RT, 2.) THF, 45 min

2: 85 percent / oxalyl chloride, DMSO / CH₂Cl₂ / 0.25 h / -70 °C

3: 1.) nBuLi / 1.) THF, hexane, 30 min, 2.) THF, hexane, a) -25 deg C, 30 min, b) 1 h, RT

4: 1.) 9-BBN, 2.) aq. H₂O₂, NaOH / 1.) THF, RT, 1 h, 2.) EtOH, 15 min

5: 78 percent / oxalyl chloride, DMSO / CH₂Cl₂ / 0.25 h / -70 °C

With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; n-butyllithium; oxalyl dichloride; dihydrogen peroxide; sodium hydride; dimethyl sulfoxide; In dichloromethane;
DOI:10.1016/0223-5234(96)88240-7