(R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

Base Information

Chemical Name:(R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide
CAS No.:1418635-75-2
Molecular Formula:C₁₃H₁₀ClNO₃S
Molecular Weight:295.746
Hs Code.:

Synonyms:(R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

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Technology Process of (R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

There total 3 articles about (R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide 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: 98.0%

: 63503-60-6
3-chlorophenylboronic acid

: 71730-46-6
benzo[e][1,2,3]oxathiazine 2,2-dioxide

: 1418635-75-2
(R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

Guidance literature:: 3-chlorophenylboronic acid; benzo[e][1,2,3]oxathiazine 2,2-dioxide; With chlorobis(cyclooctene)rhodium(I) dimer; C₁₈H₂₃NOS; In toluene; at 20 ℃; for 0.5h; Inert atmosphere;

With potassium fluoride; In water; toluene; at 20 ℃; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ja3110818

Reference yield: 98.0%

: 1025496-32-5
C₁₂H₁₀BClO₂

: 71730-46-6
benzo[e][1,2,3]oxathiazine 2,2-dioxide

: 1418635-75-2
(R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

Guidance literature:: With C₁₈H₂₃NOS; dichlorotetrakis(cyclooctene)dirhodium; In toluene; at 20 ℃; for 0.5h; enantioselective reaction;
DOI:10.1055/s-0033-1338418

Reference yield: 91.0%

: 1418635-75-2
(R)-4-(3-chlorophenyl)-3,4-dihydrobenzo[e][1,2,3]oxathiazine-2,2-dioxide

Guidance literature:: With nickel(II) perchlorate hexahydrate; (4S,5S)-2-((R)-7′-(diphenylphosphanyl)-3,3,3′,3′,5,5′-hexamethyl-2,2′,3,3′-tetrahydro-1,1′-spirobi[inden]-7-yl)-4,5-diphenyl-4,5-dihydrooxazole; In 2,2,2-trifluoroethanol; at 60 ℃; for 48h; Schlenk technique; Inert atmosphere;