125340-68-3

Usage

Uses

Used in Pharmaceutical Industry:
4-BENZYLOXY-1-CHLOROBUTANE is used as a synthetic intermediate for the development of various pharmaceutical compounds. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-BENZYLOXY-1-CHLOROBUTANE is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and functional groups enable the production of effective and targeted agrochemical products.
Used in Fine Chemicals Industry:
4-BENZYLOXY-1-CHLOROBUTANE is employed as a key building block in the synthesis of fine chemicals, which are high-purity chemicals used in various applications, including fragrances, dyes, and specialty chemicals. Its versatility in organic synthesis contributes to the development of novel and high-quality fine chemicals.
Used in Organic Synthesis Research:
As a reagent in organic synthesis, 4-BENZYLOXY-1-CHLOROBUTANE is used in research laboratories to explore new synthetic pathways and develop innovative chemical compounds. Its unique structure and reactivity make it a valuable tool for chemists in advancing the field of organic chemistry.

Upstream product

• 95672-91-6 (2S,3S)-4-benzyloxy-2,3-epoxy-1-butanol 
• 80885-30-9 (E)-4-(benzyloxy)-2-buten-1-ol 
• 78469-85-9 (2S,3S)-4-benzyloxy-2,3-epoxy-1-butanol 

Downstream Products

• 85428-24-6 (R)-4-benzyloxy-3-hydroxy-1-butyne 
• 85428-24-6 (S)-1-(benzyloxy)but-3-yn-2-ol 

Relevant academic research and scientific papers

Stereoselective total synthesis of (+)-anamarine via cross-metathesis protocol

A convergent stereoselective total synthesis of (+)-anamarine via cross-metathesis (CM) protocol starting from 2-butyn-1,4-diol and vinyl lactone is reported. Other key features of the strategy include the use of Sharpless asymmetric epoxidation, Sharples

AN ENANTIOCONTROLLED ROUTE TO THE C11-17 SEGMENT OF MYCINAMICINS III AND IV

An enantiocontrolled route to the common C11-17 segment (2) of mycinamicins III (1a) and IV (1b) has been developed starting from the chiral α-hydroxyacetylene (6) obtained from (E)-4-benzyloxybut-2-en-1-ol (3).

Enantiodivergent Route to the Aromatic Bisabolane Sesquiterpenes via a Chiral Acetylene Alcohol

Efficient preparation and practical utilization of (R)-1-benzyloxy-3-butyn-2-ol have been established.Treatment of (2S,3S)-4-benzyloxy-2,3-epoxybutyl chloride, obtained via the Sharpless epoxidation, with n-butyllithium afforded (R)-1-benzyloxy-3-butyn-2-

Asymmetric Construction of Optically Active 3-Hydroxyalkyne Functionalities

An efficient method for the construction of optically active 3-hydroxyalkyne functionalities has been developed using optically active α,β-epoxy alcohols readily accessible from non-chiral allyl alcohol precursors.