73890-73-0

  • Product Name:(S)-1-(4-CHLOROPHENYL)-1-PROPANOL
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Product Details

Purity:99%

High Purity (S)-1-(4-CHLOROPHENYL)-1-PROPANOL 73890-73-0 Good Manufacturer

  • Molecular Formula:C9H11ClO
  • Molecular Weight:170.639
  • PSA:20.23000 
  • LogP:2.78340 

73890-73-0 Relevant articles

Rhizopus arrhizus mediated SAR studies in chemoselective biotransformation of haloketones at ambient temperature

Salokhe, Prabha R.,Salunkhe, Rajeshri S.

, (2021/09/13)

We have demonstrated a green chemistry a...

Towards practical earth abundant reduction catalysis: Design of improved catalysts for manganese catalysed hydrogenation

Widegren, Magnus B.,Clarke, Matthew L.

, p. 6047 - 6058 (2019/11/14)

Manganese catalysts derived from trident...

Chirality-Economy Catalysis: Asymmetric Transfer Hydrogenation of Ketones by Ru-Catalysts of Minimal Stereogenicity

Chen, Fumin,He, Dongxu,Chen, Li,Chang, Xiaoyong,Wang, David Zhigang,Xu, Chen,Xing, Xiangyou

, p. 5562 - 5566 (2019/06/05)

This manuscript describes the design and...

Axially chiral tridentate isoquinoline derived ligands for diethylzinc addition to aldehydes

Sweetman, Brian A.,Guiry, Patrick J.

, p. 5567 - 5581 (2018/08/09)

The synthesis and resolution of new trid...

73890-73-0 Process route

diethylzinc
557-20-0

diethylzinc

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

(R)-1-(4-chlorophenyl)-1-propanol
110611-21-7

(R)-1-(4-chlorophenyl)-1-propanol

(S)-1-(4-chlorophenyl)-1-propanol
73890-73-0

(S)-1-(4-chlorophenyl)-1-propanol

para-Chlorobenzyl alcohol
873-76-7

para-Chlorobenzyl alcohol

Conditions
Conditions Yield
With (1S)-(+)-3-exo-(dimethylamino)isoborneol; In toluene; at 0 ℃; for 12h; Yields of byproduct given. Title compound not separated from byproducts;
2%
86%
With polymer-supported camphor derivative; In toluene; at 20 ℃; Title compound not separated from byproducts;
13%
With (P,P)-(+)-bis[5]helicene diol; In toluene; for 24h; Title compound not separated from byproducts;
 
With chiral bicyclo[3.2.1]octane-based alcohol; In hexane; toluene; at 20 ℃; for 24h; Title compound not separated from byproducts;
 
With (-)-8-(9H-fluoren-9-ylidene)-1-(2-hydroxyphenyl)-7-methyl-5,6,7,8-tetrahydronaphthalen-2-ol; In hexane; toluene; at 0 ℃; for 168h; enantioselective reaction; Schlenk technique; Inert atmosphere;
35 % ee
With (-)-8-(9H-fluoren-9-ylidene)-1-(2-hydroxyphenyl)-7-methyl-5,6,7,8-tetrahydronaphthalen-2-ol; In hexane; toluene; at 0 ℃; for 168h; enantioselective reaction; Schlenk technique; Inert atmosphere;
24 % ee
triethylaluminum
97-93-8

triethylaluminum

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

(R)-1-(4-chlorophenyl)-1-propanol
110611-21-7

(R)-1-(4-chlorophenyl)-1-propanol

(S)-1-(4-chlorophenyl)-1-propanol
73890-73-0

(S)-1-(4-chlorophenyl)-1-propanol

para-Chlorobenzyl alcohol
873-76-7

para-Chlorobenzyl alcohol

Conditions
Conditions Yield
triethylaluminum; With titanium(IV) isopropylate; L-3-phenyllactic acid; In tetrahydrofuran; toluene; at 21 ℃; for 4h;
4-chlorobenzaldehyde; In tetrahydrofuran; toluene; at 21 ℃; for 4h; Title compound not separated from byproducts;
 

73890-73-0 Upstream products

  • 557-20-0
    557-20-0

    diethylzinc

  • 104-88-1
    104-88-1

    4-chlorobenzaldehyde

  • 97-93-8
    97-93-8

    triethylaluminum

  • 123-11-5
    123-11-5

    4-methoxy-benzaldehyde

73890-73-0 Downstream products

  • 1430475-51-6
    1430475-51-6

    C12H15ClO2